-
question_answer1)
Two crosses between the same pair of genotypes of phenotypes in which the sources of the gametes are reversed in one cross is known as:
A)
Test cross done
clear
B)
Dihybrid cross done
clear
C)
Reverse cross done
clear
D)
Reciprocal cross done
clear
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question_answer2)
The total number of progenies obtained through dihybrid cross of Mendel is 1280 in F2 generation. How many are recombinants?
A)
240 done
clear
B)
360 done
clear
C)
480 done
clear
D)
720 done
clear
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question_answer3)
What is shown in the following figure? |
|
A)
Steps in making a selfing in a pea plant done
clear
B)
Steps in making a cross in a lotus plant done
clear
C)
Steps in making a cross in a pea plant done
clear
D)
Steps in making a cross in a rose plant done
clear
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question_answer4)
In Mendel's experiments with garden pea, round seed shape (RR) was dominant over wrinkled seeds (rr), yellow cotyledon (YY) was dominant over green cotyledon (yy). What are the expected phenotypes in the \[{{F}_{2}}\] generation of the cross \[RRYY\text{ }\times \text{ }rryy\text{ }?\]
A)
Only round seeds with green cotyledon done
clear
B)
Only wrinkled seeds with yellow cotyledons done
clear
C)
Only wrinkled seeds with green cotyledons done
clear
D)
Round seeds with yellow cotyledons, and wrinkled seeds with yellow cotyledons done
clear
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question_answer5)
How many different kinds of gametes will be produced by a plant having the genotype AA Bb CC ?
A)
Three done
clear
B)
Four done
clear
C)
Nine done
clear
D)
Two done
clear
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question_answer6)
The possible blood group of children born to parents having A and AB groups are :
A)
0, A done
clear
B)
A, B, AB done
clear
C)
0, A, B done
clear
D)
0, A, B, AB done
clear
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question_answer7)
In Mirabilis jalapa, the number of \[{{F}_{2}}\] red flowered plants in a cross of red flowered x white flowered would be :
A)
1 done
clear
B)
2 done
clear
C)
3 done
clear
D)
4 done
clear
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question_answer8)
What type of cross is shown in the following figure? |
|
A)
Diagrammatic representation of dihybrid cross done
clear
B)
Diagrammatic representation of trihybrid cross done
clear
C)
Diagrammatic representation of monohybrid cross done
clear
D)
Diagrammatic representation of test cross done
clear
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question_answer9)
A common test to find the genotype of a hybrid is by :
A)
Crossing of one \[{{F}_{2}}\] progeny with female parent done
clear
B)
Studying of sexual behaviour of \[{{F}_{1}}\] progenies done
clear
C)
Crossing of one \[{{F}_{1}}\] progeny with male parent done
clear
D)
Crossing of one \[{{F}_{2}}\] progeny with male parent done
clear
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question_answer10)
One of the parents of a cross has mutation in its mitochondria. In that cross, the parent is taken as male. During segregation of \[{{F}_{2}}\] progenies that mutation is found in :
A)
One third of the progenies done
clear
B)
None of the progenies done
clear
C)
All of the progenies done
clear
D)
Fifty per cent of the progenies done
clear
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question_answer11)
In the ABO system of blood groups, if both antigens are present but no antibody, the blood group the individual would be :
A)
B done
clear
B)
0 done
clear
C)
AB done
clear
D)
A done
clear
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question_answer12)
Extranuclear inheritance is a consequence of presence of genes in :
A)
Mitochondria and chloroplasts done
clear
B)
Endoplasmic reticulum and mitochondria done
clear
C)
Ribosomes and chloroplasts done
clear
D)
Lysosomes and ribosomes done
clear
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question_answer13)
Which one of the following characters studied by Mendel in garden pea was found to be dominant?
A)
Green seed colour done
clear
B)
Terminal flower position done
clear
C)
Green pod colour done
clear
D)
Wrinkled seed done
clear
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question_answer14)
In a given plant red colour (R) of fruits is dominant over white fruit (r); tallness (T) is dominant over dwarfness (t). If a plant with genotype RRTt is crossed with a plant of genotype rrtt, what will be the percentage of tall plants with red fruits in the next generation?
A)
100% done
clear
B)
25% done
clear
C)
50% done
clear
D)
75% done
clear
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question_answer15)
If a dwarf pea plant was treated with gibberellic acid, it became a tall, as tall pea plants. If these pea plants are crossed with pure tall pea plants, what will be the phenotypic ratio in \[{{F}_{1}}\]generation?
A)
All dwarf plants done
clear
B)
50% tall and 50% dwarf plants done
clear
C)
75 % tall and 25 % dwarf plants done
clear
D)
100% tall plants done
clear
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question_answer16)
Red (dominant) flowered heterozygous crossed with white flower :
A)
\[350\text{ }-\text{ }red\text{ }:\text{ }350\text{ }\tilde{\ }\text{ }white\] done
clear
B)
\[450\text{ }-\text{ }red\text{ }:\text{ }250\text{ }\tilde{\ }\text{ }white\] done
clear
C)
\[380\text{ }-\text{ }red\text{ }:\text{ }250\text{ }\tilde{\ }\text{ }white\] done
clear
D)
None of the above done
clear
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question_answer17)
A tall plant was grown in nutrient deficient soil and remained dwarf. When it is crossed with dwarf plant then :
A)
All hybrid plants are dwarf done
clear
B)
All hybrid plants are tall done
clear
C)
50% tall and 50% of dwarf done
clear
D)
75% tall and 25% dwarf done
clear
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question_answer18)
A pure tall and a pure dwarf plant were crossed to produce offspring. Offsprings were self crossed, then find out the ratio between true breeding tall to true breeding dwarf?
A)
1 : 1 done
clear
B)
3 : 1 done
clear
C)
2 : 1 done
clear
D)
1 : 2 : 1 done
clear
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question_answer19)
Cross between unrelated group of organisms is called :
A)
Hybrid done
clear
B)
Test cross done
clear
C)
Back cross done
clear
D)
Heterosis done
clear
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question_answer20)
Cytoplasmic inheritance is due to : |
(1) Mitochondria and Chloroplast |
(2) Cilia and Flagella |
(3) Cytoplasmic particles |
(4) Cell wall and Cell coat |
A)
1, 2 and 3 are correct done
clear
B)
1 and 2 are correct done
clear
C)
2 and 4 are correct done
clear
D)
1 and 3 are correct done
clear
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question_answer21)
Mating of an organism to a double recessive in order to determine whether it is homozygous or heterozygous for a character under consideration is called :
A)
Reciprocal cross done
clear
B)
Test cross done
clear
C)
Dihybrid cross done
clear
D)
Back cross done
clear
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question_answer22)
What is depicted in the following cross? |
|
A)
Diagrammatic representation of test cross done
clear
B)
Diagrammatic representation of out cross done
clear
C)
Diagrammatic representation of reverse cross done
clear
D)
Diagrammatic representation of dihybrid cross done
clear
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question_answer23)
The phenotypic ratio in the \[{{F}_{2}}\] generation of a dihybrid cross is :
A)
9 : 3 : 3 : 1 done
clear
B)
1 : 2 : 2 : 4 : 1 : 2 : 1 : 2 : 1 done
clear
C)
7 : 1 : 1 : 7 done
clear
D)
1 : 2 : 3 : 4 done
clear
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question_answer24)
A woman is married for the second time. Her first husband was ABO blood type A, and her child by that marriage was type O. Her new husband is type B and their child is type AB. What is the woman's ABO genotype and blood type?
A)
\[{{I}^{A}}{{I}^{O}}\]; Blood type A done
clear
B)
\[{{I}^{A}}{{I}^{B}}\]; Blood type AB done
clear
C)
\[{{I}^{B}}{{I}^{O}}\]; Blood type B done
clear
D)
\[{{I}^{O}}{{I}^{O}}\]; Blood type O done
clear
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question_answer25)
Codominance is depicted by
A)
B blood group done
clear
B)
AB blood group done
clear
C)
O blood group done
clear
D)
A blood group done
clear
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question_answer26)
The ABO blood grouping in human beings is an example for : |
(i) Dominance |
(ii) Incomplete dominance |
(iii) Co-dominance |
(iv) Multiple alleles |
A)
(i) and (ii) only done
clear
B)
(ii), (iii) and (iv) done
clear
C)
(i) (ii) and (iv) done
clear
D)
(iii) and (iv) only done
clear
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question_answer27)
Which of the following genotypes does not produce an sugar polymer on the surface of the RBC ?
A)
\[{{I}^{A}}{{I}^{A}}\] done
clear
B)
\[I{{i}^{B}}\] done
clear
C)
\[{{I}^{A}}{{I}^{B}}\] done
clear
D)
ii done
clear
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question_answer28)
Inheritance of flower colour is an example of incomplete dominance which is seen in :
A)
Antirrhinum done
clear
B)
Pisum done
clear
C)
Solanum done
clear
D)
Hibiscus done
clear
View Solution play_arrow
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question_answer29)
Phenotypic ratio in plant Snapdragon in \[{{F}_{2}}\] is :
A)
1 : 1 done
clear
B)
2 : 1 done
clear
C)
3 : 1 done
clear
D)
1 : 2 : 1 done
clear
View Solution play_arrow
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question_answer30)
Test cross is used to :
A)
Check heterozygosity in \[{{F}_{1}}\] generation done
clear
B)
Check heterozygosity in \[{{F}_{2}}\] generation done
clear
C)
Check independent assortment in \[{{F}_{2}}\] generation done
clear
D)
Check segregation in \[{{F}_{2}}\] generation done
clear
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question_answer31)
The ultimate biological unit which controls heredity is called :
A)
Genome done
clear
B)
Chromosome done
clear
C)
Genotype done
clear
D)
Gene done
clear
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question_answer32)
For making important contributions in respect of the nature of genes, the Nobel prize was awarded :
A)
T.H. Morgan done
clear
B)
de Vries done
clear
C)
H.J. Muller done
clear
D)
Darwin done
clear
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question_answer33)
A pea plant parent having violet coloured flowers with unknown genotype was crossed with a plant having white coloured flowers, in the progeny 50% of the flowers were violet and 50% were white. The genotypic constitution of the parent having violet coloured flowers was:
A)
Homozygous done
clear
B)
Merozygous done
clear
C)
Heterozygous done
clear
D)
Hemizygous done
clear
View Solution play_arrow
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question_answer34)
Find out the correct option regarding the following cross? |
|
A)
Monohybrid cross in pea plant done
clear
B)
Trihybrid cross in pea plant done
clear
C)
Out cross in pea plant done
clear
D)
Dihybrid cross in pea plant done
clear
View Solution play_arrow
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question_answer35)
ABO blood group is based on :
A)
Co-dominance done
clear
B)
Incomplete dominance done
clear
C)
Epistasis done
clear
D)
Multiple allele done
clear
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question_answer36)
Test cross of dihybrid ratio is 1 : 1 : 1 : 1. It proves that :
A)
\[{{F}_{1}}\] hybrid produces four different progenies done
clear
B)
\[{{F}_{2}}\] hybrid is homozygous done
clear
C)
Two different progenies are produced by \[{{P}_{1}}\] parents done
clear
D)
\[{{F}_{2}}\] hybrid is heterozygous done
clear
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question_answer37)
If \[{{F}_{1}}\] generation has all tall progenies and ratio of \[{{F}_{2}}\] generation is 3 : 1 (Tall : Dwarf), then it proves:
A)
Law of independent assortment done
clear
B)
Law of segregation done
clear
C)
Law of dominance done
clear
D)
Incomplete dominance done
clear
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question_answer38)
How many pairs of contrasting characters in pea pod were chosen by Mendel :
A)
3 done
clear
B)
5 done
clear
C)
7 done
clear
D)
9 done
clear
View Solution play_arrow
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question_answer39)
If a cross between two individual produce offsprings with 50% dominant character [A] and 50% recessive character [A] the genotype of parents are :
A)
Aa AA done
clear
B)
Aa aa done
clear
C)
AA aa done
clear
D)
AA Aa done
clear
View Solution play_arrow
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question_answer40)
When yellow round heterozygous pea plants are self-fertilized, the frequency of occurrence of RrYY genotype among the offsprings is
A)
9/16 done
clear
B)
3/16 done
clear
C)
2/16 done
clear
D)
1/16 done
clear
View Solution play_arrow
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question_answer41)
In an organism, tall phenotype is dominant over recessive dwarf phenotype, and the alleles are designate as T and t, respectively. Upon crossing two different individuals, total 250 offsprings were obtained. out of which 124 displayed tall phenotype and rest were dwarf. Thus, the genotype of the parents was
A)
\[TT\times TT\] done
clear
B)
\[TT\times tt\] done
clear
C)
\[Tt\times Tt\] done
clear
D)
\[Tt\times tt\] done
clear
View Solution play_arrow
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question_answer42)
In a monohybrid cross between two heterozygous individuals, the number of pure homozygous individual? obtained in \[{{F}_{1}}\] generation is
A)
2 done
clear
B)
4 done
clear
C)
6 done
clear
D)
8 done
clear
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question_answer43)
A woman with blood type 'O' has a child with blood type 'O'. If she claims a friend of hers with blood group 'A' as the father of the child, then the genotype of the father would be
A)
\[{{I}^{O}}{{I}^{O}}\] done
clear
B)
\[{{I}^{A}}{{I}^{B}}\] done
clear
C)
\[{{I}^{A}}{{I}^{O}}\] done
clear
D)
\[{{I}^{A}}{{I}^{O}}\] done
clear
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question_answer44)
A woman with straight hair mates with a man with curly hair who is known to be heterozygous for that trait. What is the chance that their first child will have curly hair?
A)
No chance done
clear
B)
One in two done
clear
C)
It is certain done
clear
D)
One in four done
clear
View Solution play_arrow
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question_answer45)
Which of the following crosses and resultant phenotype ratios are mismatched?
A)
\[Tt\times Tt-3\,:\,1\] done
clear
B)
\[tt\times Tt-2\,;\,1\] done
clear
C)
\[Tt\,\,Yy\,\,\times \,\,ttyy\,\,-\,\,1\,\,:\,\,1\,\,:\,\,1\,\,:\,\,1\] done
clear
D)
\[Tt\,Yy\,\times \,\,TtYy\,\,\,-\,9\,\,:\,\,3\,\,:\,\,3\,\,:\,\,\,1\] done
clear
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question_answer46)
A man having the genotype EEFfGgHH can produce P number of genetically different sperms, and a woman of genotype IuLLMmNn can generate Q number of genetically different eggs. Determine the values of P and Q
A)
P = 4, q = 4 done
clear
B)
P = 4, q = 6 done
clear
C)
P = 8, q = 4 done
clear
D)
P = 8, q = 8 done
clear
View Solution play_arrow
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question_answer47)
An organism, tall phenotype is dominant over recessive dwarf phenotype, and the alleles are designated as T and t, respectively. Upon crossing two different individuals, total 250 offsprings were obtained. out of which 124 displaced tall phenotype and rest were dwarf. Thus, the genotype of the parent; were
A)
\[TT\,\,\,\times \,\,\,TT\] done
clear
B)
\[TT\,\,\,\times \,\,\,tt\] done
clear
C)
\[Tt\,\,\,\times \,\,\,Tt\] done
clear
D)
\[Tt\,\,\,\times \,\,\,tt\] done
clear
View Solution play_arrow
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question_answer48)
When yellow round heterozygous pea plants are self-fertilized, the frequency of occurrence of RrYY genotype, among the offsprings is
A)
9/16 done
clear
B)
3/16 done
clear
C)
2/16 done
clear
D)
1/16 done
clear
View Solution play_arrow
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question_answer49)
ABO blood groups are determined by three different alleles. How many genotypes and phenotypes are possible?
A)
B)
C)
D)
View Solution play_arrow
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question_answer50)
In a monohybrid cross between two heterozygous individuals, the number of pure homozygous individuals obtained in \[{{F}_{1}}\] generation is
A)
2 done
clear
B)
4 done
clear
C)
6 done
clear
D)
8 done
clear
View Solution play_arrow
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question_answer51)
In Mendel's seven contrasting traits of pea total number of colours tested by him was
A)
2 done
clear
B)
3 done
clear
C)
4 done
clear
D)
5 done
clear
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question_answer52)
Which of the following statements is correct?
A)
Each back cross is a test cross. done
clear
B)
Each test cross is a back cross. done
clear
C)
Crossing \[{{F}_{2}}\] with \[{{F}_{1}}\] is a test cross. done
clear
D)
Crossing \[{{F}_{2}}\] with \[{{P}_{1}}\] is called a test cross. done
clear
View Solution play_arrow
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question_answer53)
If a heterozygous tall plant is crossed with a homozygous dwarf plant, the proportion of dwarf progeny will be
A)
25% done
clear
B)
50% done
clear
C)
75% done
clear
D)
100% done
clear
View Solution play_arrow
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question_answer54)
An allele is
A)
Another word for gene done
clear
B)
A homozygous genotype done
clear
C)
A heterozygous genotype done
clear
D)
One of the several possible forms of gene done
clear
View Solution play_arrow
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question_answer55)
The graphical representation to calculate the probability of all possible genotypes of offsprings in a genetic cross was developed by
A)
Gregor Mendel done
clear
B)
Kornberg done
clear
C)
Har Gobind Khorana done
clear
D)
Reginald C. Punnett done
clear
View Solution play_arrow
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question_answer56)
Choose the wrong statement from the following.
A)
Failure of segregation of chromatids during cell division results in aneuploidy done
clear
B)
Additional copy of 'X' chromosome in males results in Klinefelter's syndrome done
clear
C)
Closely located genes in a chromosome always assort independently resulting in recombinants done
clear
D)
According to Mendel, recessive character never blends in heterozygous condition done
clear
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question_answer57)
In garden pea, round shape of seeds is dominant over wrinkled shape. A pea plant heterozygous for round shape of seed is selfed and 1600 seeds produced during the cross are subsequently germinated. How many seedings would have the parental phenotype?
A)
400 done
clear
B)
1600 done
clear
C)
1200 done
clear
D)
800 done
clear
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question_answer58)
In a plant species, flower colour yellow is dominant over white, and fruit shape round is dominant over elongated. Crossing was performed between two pure lines - one having yellow-flower and round fruit, and another with white-flower and elongated-fruit. About 20 plants survived in \[{{F}_{1}}\] progeny. Plants of \[{{F}_{1}}\] were allowed to self fertilize, and about 960 plants survived in \[{{F}_{2}}\]. If the traits follow Mendelian inheritance, the number of plants would have yellow flower and round fruit in \[{{F}_{1}}\] and \[{{F}_{2}}\] are respectively
A)
20, 960 done
clear
B)
20, 540 done
clear
C)
10, 180 done
clear
D)
10, 60 done
clear
View Solution play_arrow
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question_answer59)
Two plants one with black flower and other with white coloured flower were crossed in an experiment. In the next generation grey coloured flowers were obtained. The reason for the result is
A)
incomplete dominance done
clear
B)
pseudodominance done
clear
C)
codominance done
clear
D)
None of these done
clear
View Solution play_arrow
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question_answer60)
Genes which code for a pair of contrasting characters are called
A)
factors done
clear
B)
traits done
clear
C)
alleles done
clear
D)
gametes done
clear
View Solution play_arrow
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question_answer61)
First husband of Asha had ABO blood type A and their child had type O. She remarried and her second husband had ABO blood type B and their child had type AB. What is the ABO genotype of Asha and also name her blood type?
A)
ii; Blood type O done
clear
B)
\[{{I}^{B}}\,\,i\] ; Blood type B done
clear
C)
\[{{I}^{A}}{{I}^{B}}\]; Blood type AB done
clear
D)
\[{{I}^{A}}\,\,i\] ; Blood type A done
clear
View Solution play_arrow
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question_answer62)
During incomplete dominance, \[{{F}_{2}}\] generation will have
A)
3 : 1 genotypic ratio done
clear
B)
3 : 1 phenotypic ratio done
clear
C)
1 : 2 : 1 genotypic ratio done
clear
D)
2 : 2 : 1 phenotypic ratio done
clear
View Solution play_arrow
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question_answer63)
Which of the following cross will give recessive progeny in \[{{F}_{1}}\] generation?
A)
\[TT\,\,\,\,\times \,\,\,\,\,tt\] done
clear
B)
\[Tt\,\,\,\,\,\times \,\,\,\,TT\] done
clear
C)
\[tt\,\,\,\,\,\times \,\,\,\,\,tt\] done
clear
D)
\[TT\,\,\,\,\,\times \,\,\,\,\,\,TT\] done
clear
View Solution play_arrow
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question_answer64)
In a dihybrid cross between two heterozygotes \[AaBb\,\,\times \,\,Aa\,\,Bb\], if we get 3 : 1 ratio among the offsprings, the reason for this may be
A)
polygenes done
clear
B)
linked genes done
clear
C)
pleiotropic genes done
clear
D)
hypostatic genes done
clear
View Solution play_arrow
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question_answer65)
What result Mendel would have got, had he self-pollinated a tall \[{{F}_{2}}\] plant?
A)
TT and Tt done
clear
B)
All Tt done
clear
C)
All TT done
clear
D)
All tt done
clear
View Solution play_arrow
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question_answer66)
Test cross is a cross between
A)
Hybrid \[\times \] dominant parent done
clear
B)
Hybrid \[\times \] recessive parent done
clear
C)
Hybrid \[\times \] hybrid parent done
clear
D)
Two distantly related species done
clear
View Solution play_arrow
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question_answer67)
Colchicine interferes with
A)
Chromosome replication done
clear
B)
Organisation of spindle done
clear
C)
Chromosome condensation done
clear
D)
Incorporation of nitrogen base done
clear
View Solution play_arrow
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question_answer68)
Webbed neck is a characteristic of
A)
XXY done
clear
B)
XY done
clear
C)
XXY done
clear
D)
XO done
clear
View Solution play_arrow
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question_answer69)
Daughter of a colour-blind father and normal mother marries a colour-blind person. Colour-blindness in the family shall be
A)
50% sons and 50% daughters done
clear
B)
All sons and daughters done
clear
C)
All daughters done
clear
D)
All sons done
clear
View Solution play_arrow
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question_answer70)
What are depicted in the following figure of chromosome? |
|
A)
Dependent assortment of chromosomes done
clear
B)
Independent assortment of Chromatin done
clear
C)
Independent assortment of chromosomes done
clear
D)
Dependent assortment of Chromatin done
clear
View Solution play_arrow
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question_answer71)
Which one of the following statements is correct?
A)
Down's syndrome occurs mostly in the children of very young mothers done
clear
B)
A person suffering from Down's syndrome has 47 chromosomes done
clear
C)
Down's syndrome is very common and occurs once is every 50 births done
clear
D)
Down's syndrome is caused when a sperm with an extra X chromosome fuses with a normal egg done
clear
View Solution play_arrow
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question_answer72)
Recessive characters are expressed when present:
A)
Only when they are present on X chromosome of male done
clear
B)
Only when they are present on X chromosomes of female done
clear
C)
On any of autosome done
clear
D)
On any one chromosome done
clear
View Solution play_arrow
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question_answer73)
"Hypertrichosis" hairy ears are a sex-linked character associated with the
A)
X chromosome done
clear
B)
XX chromosome done
clear
C)
XY chromosome done
clear
D)
Y chromosome done
clear
View Solution play_arrow
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question_answer74)
If this type of chromosome combination is found in man, we call this the "Klinefelter's syndrome"
A)
One "X" chromosome and two "Y" chromosomes (XYY) done
clear
B)
Three "X" chromosomes (XXX) done
clear
C)
Three "Y" chromosomes (YYY) done
clear
D)
Two "X" chromosomes and one "Y" chromosome (XXY) done
clear
View Solution play_arrow
-
question_answer75)
Mongoloid syndrome or Mongolian Idiocy is due to
A)
21 pairs normal, 22 and 23 extra chromosomes done
clear
B)
22 pairs are normal, one chromosome has trisomy done
clear
C)
24 pairs normal and one extra chromosome done
clear
D)
22 pairs of normal chromosomes with one X chromosome done
clear
View Solution play_arrow
-
question_answer76)
The exchange of generic material between chromatids of paired homologous chromosomes during first meiotic division is called
A)
Transformation done
clear
B)
Chiasmata done
clear
C)
Crossing over done
clear
D)
Synapsis done
clear
View Solution play_arrow
-
question_answer77)
Sex factor in bacteria
A)
Chromosomal replicon done
clear
B)
F-Factor done
clear
C)
RNA - Fimbrae done
clear
D)
Sex-pilus done
clear
View Solution play_arrow
-
question_answer78)
A person with 47 chromosomes due to an additional Y chromosome suffers from a condition called
A)
Down's syndrome done
clear
B)
Super male done
clear
C)
Turner's syndrome done
clear
D)
Klinefelter's syndrome done
clear
View Solution play_arrow
-
question_answer79)
For evolutionary success, a mutation must occur in
A)
Germplasm DNA done
clear
B)
Somatic RNA done
clear
C)
Germplasm RNA done
clear
D)
Somatic DNA done
clear
View Solution play_arrow
-
question_answer80)
Sometimes chromosome number increase or decrease due to:
A)
Non-disjunction of chromosome done
clear
B)
Genetic repetition done
clear
C)
Mutation done
clear
D)
All of these done
clear
View Solution play_arrow
-
question_answer81)
The pedigree chart given below shows a particular trait which is absent in parents but present in the next generation irrespective of sexes. Draw your conclusion on the basis of the pedigree. |
|
A)
Allosome linked and recessive in nature done
clear
B)
Autosome linked and dominent in nature done
clear
C)
Allosome linked and dominent in nature done
clear
D)
Autosome linked and recessive in nature done
clear
View Solution play_arrow
-
question_answer82)
Mutations are mainly responsible for controlling :
A)
Increasing population rate done
clear
B)
Maintaining genetic continuity done
clear
C)
Variation in organisms done
clear
D)
Extinction of organisms done
clear
View Solution play_arrow
-
question_answer83)
A woman with two genes, one for haemophilia and a gene for colour blindness on one of the 'X' chromosomes marries a normal man. Progeny will be :
A)
All sons and daughters haemophilic and colour-blind done
clear
B)
Haemophilic and colour-blind daughters done
clear
C)
50% haemophilic colour-blind sons and 50% normal sons done
clear
D)
50% haemophilic daughters and 50% colour-blind daughters done
clear
View Solution play_arrow
-
question_answer84)
In Down's syndrome, karyotyping has shown that the disorder is associated with trisomy of chromosome number 21 usually due to
A)
Addition of extra chromosome during mitosis of the zygote done
clear
B)
Non-disjunction during egg-cell formation done
clear
C)
Non-disjunction during sperm-cell formation done
clear
D)
Non-disjunction during formation of egg cells and sperm-cells done
clear
View Solution play_arrow
-
question_answer85)
Mental retardation in man associated with sex chromosomal abnormality is usually due to :
A)
Reduction in X complement done
clear
B)
Increase in X complement done
clear
C)
Moderate increase in Y complement done
clear
D)
Large increase in Y complement done
clear
View Solution play_arrow
-
question_answer86)
Albinism is known to be due to an autosomal recessive mutation. The first child of a couple with normal skin pigmentation was an albino. What is the probability that their second child will also be an albino?
A)
100% done
clear
B)
25% done
clear
C)
50% done
clear
D)
75% done
clear
View Solution play_arrow
-
question_answer87)
One of the chief factors responsible for clotting of blood is present on :
A)
X Chromosome of male only done
clear
B)
X Chromosome of female only done
clear
C)
X Chromosome of both male and female done
clear
D)
Autosomes only done
clear
View Solution play_arrow
-
question_answer88)
What is shown in the following figure of pedigrees? |
|
A)
Autosomal recessive trait like myotonic dystrophy done
clear
B)
Allosomal dominant trait like myotonic dystrophy done
clear
C)
Autosomal dominant trait like myotonic dystrophy done
clear
D)
Autosomal dominant trait like sickle - cell anaemia done
clear
View Solution play_arrow
-
question_answer89)
A colour-blind daughter is born when :
A)
Father is colour-blind, mother is normal done
clear
B)
Mother is colour-blind, father is normal done
clear
C)
Mother is carrier, father is normal done
clear
D)
Mother is carrier, father is colour-blind done
clear
View Solution play_arrow
-
question_answer90)
In Down's syndrome (Mongolism) each cell has how many chromosomes:
A)
21st pair having one less done
clear
B)
23rd pair with one less done
clear
C)
45 chromosomes done
clear
D)
47 chromosomes done
clear
View Solution play_arrow
-
question_answer91)
Where are Barr bodies found?
A)
Sperms of a man done
clear
B)
Ova of a woman done
clear
C)
Body cells (somatic) of man done
clear
D)
Body cells (somatic) of woman done
clear
View Solution play_arrow
-
question_answer92)
The hereditary material present in the bacterium Escherichia coli is :
A)
Single stranded DNA done
clear
B)
Single stranded RNA done
clear
C)
Double stranded DNA done
clear
D)
Double stranded RNA done
clear
View Solution play_arrow
-
question_answer93)
Extranuclear genes occur in which of the following:
A)
Mitochondria and cytoplasm done
clear
B)
Ribosomes and cytoplasm done
clear
C)
ER and cytoplasm done
clear
D)
Cytoplasm and Lysosomes done
clear
View Solution play_arrow
-
question_answer94)
Mutations generally occur in which of the following genes:
A)
Dominant genes done
clear
B)
Recessive genes done
clear
C)
Lethal genes done
clear
D)
Mendel's genes done
clear
View Solution play_arrow
-
question_answer95)
Significance of the telomere is that it :
A)
Seals the chromosome done
clear
B)
Stretches the spindle fibres done
clear
C)
Synthesises proteins done
clear
D)
All of these done
clear
View Solution play_arrow
-
question_answer96)
Plasmids are useful in genetic engineering because they :
A)
Replicate independently done
clear
B)
Carry useful genes done
clear
C)
Are common in eukaryotes done
clear
D)
Can be extracted from viruses done
clear
View Solution play_arrow
-
question_answer97)
Strength of linkage is inversely proportional to distance between the :
A)
Chromomeres done
clear
B)
Genes done
clear
C)
Telomeres done
clear
D)
Chromatids done
clear
View Solution play_arrow
-
question_answer98)
If a group of genes are getting deleted and undergoing some change it is due to :
A)
Gene mutation done
clear
B)
Aneuploidy done
clear
C)
Chromosomal mutation done
clear
D)
Gene modification done
clear
View Solution play_arrow
-
question_answer99)
XX male and XY female are very rare in humans. They are due to :
A)
Genes of Y-chromosome are on X chromosome done
clear
B)
Crossing over between X and Y done
clear
C)
Non-disjunction of chromosomes done
clear
D)
All of the above done
clear
View Solution play_arrow
-
question_answer100)
Which of the following occurs more than one and less than five in chromosome?
A)
Chromomere done
clear
B)
Chromatid done
clear
C)
Centromere done
clear
D)
Secondary constriction done
clear
View Solution play_arrow
-
question_answer101)
Change in sequence of nucleotide in DNA plant is:
A)
Mutation done
clear
B)
Isolation done
clear
C)
Polyploidy done
clear
D)
Sexual reproduction done
clear
View Solution play_arrow
-
question_answer102)
The segment of DNA which participates in crossing over is known as :
A)
Muton done
clear
B)
Cistron done
clear
C)
Recon done
clear
D)
Replicon done
clear
View Solution play_arrow
-
question_answer103)
Trisomy is :
A)
One chromosome less than 2n. done
clear
B)
One chromosome more than 2n done
clear
C)
A hybrid obtained by crossing diploid and tetraploid done
clear
D)
Three chromosomes more than 2n done
clear
View Solution play_arrow
-
question_answer104)
Kappa particles in Paramecium are indicating:
A)
Nuclear inheritance done
clear
B)
Cytoplasmic inheritance done
clear
C)
Nucleo-cytoplasmic inheritance done
clear
D)
Mutation done
clear
View Solution play_arrow
-
question_answer105)
Major role of colchicine in the eukaryotic cell is in :
A)
Reducing number of chiasmata done
clear
B)
Causing endoduplication done
clear
C)
Dividing the nucleus done
clear
D)
Formation of polytene chromosome done
clear
View Solution play_arrow
-
question_answer106)
The genes present exclusively on the X-chromosome in humans is concerned with :
A)
Baldness and trichosis done
clear
B)
Night-blindness done
clear
C)
Facial hair and moustaches in males done
clear
D)
Red-green colour blindness done
clear
View Solution play_arrow
-
question_answer107)
Down's syndrome is caused by an extra copy of chromosome number 21. What percentage of offsprings produced by an affected mother and normal father would be affected by this disorder?
A)
75% done
clear
B)
50% done
clear
C)
25% done
clear
D)
100% done
clear
View Solution play_arrow
-
question_answer108)
Linkage map of X-chromosome of fruit fly has 66 units, with yellow body gene (y) at one end and bobbed hair [b] gene at the other end. The recombination frequency between these two genes (y and b) should be :
A)
> 75% done
clear
B)
< 50% done
clear
C)
100% done
clear
D)
66% done
clear
View Solution play_arrow
-
question_answer109)
Genetic map of a eukaryotic cell is one that :
A)
Shows the stages during cell division done
clear
B)
Establishes various stages in gene evolution done
clear
C)
Establishes sites of genes on a chromosome done
clear
D)
Shows the distribution of various species in a region done
clear
View Solution play_arrow
-
question_answer110)
Genes for cytoplasmic male sterility in plants are generally located in :
A)
Cytosol done
clear
B)
Nuclear genome done
clear
C)
Chloroplast genome done
clear
D)
Mitochondrial genome done
clear
View Solution play_arrow
-
question_answer111)
When a diploid female plant (2n) is crossed with a tetraploid male plant (4n), then ploidy of endosperm cells in the resulting seed is :
A)
Triploidy done
clear
B)
Diploidy done
clear
C)
Pentaploidy done
clear
D)
Tetraploidy done
clear
View Solution play_arrow
-
question_answer112)
After the mutation at a genetic locus, the character of an organism changes due to change in :
A)
DNA replication done
clear
B)
Protein structure done
clear
C)
RNA transcription pattern done
clear
D)
Protein synthesis pattern done
clear
View Solution play_arrow
-
question_answer113)
One of the parents of a cross has a mutation in its mitochondria segregation of F2 progenies, mutaticz is found in :
A)
All the progenies done
clear
B)
None of the progenies done
clear
C)
One-third of the progenies done
clear
D)
Fifty percent of progenies done
clear
View Solution play_arrow
-
question_answer114)
Lack of independent assortment of genes A and B in fruit fly Drosophila is due to :
A)
Repulsion done
clear
B)
Linkage done
clear
C)
Crossing over done
clear
D)
Recombination done
clear
View Solution play_arrow
-
question_answer115)
Given below is the representation of a kind of chromosomal mutation. What is kind of mutation represented |
|
A)
Deletion done
clear
B)
Duplication done
clear
C)
Inversion done
clear
D)
Translocation done
clear
View Solution play_arrow
-
question_answer116)
Haemophilia is more commonly seen in human males than in human females because :
A)
A greater proportion of girls die in infancy done
clear
B)
This disease is due to an Y linked recessive mutation done
clear
C)
This disease is due to an X linked recessive mutant done
clear
D)
This disease is due to an X linked dominant mutation done
clear
View Solution play_arrow
-
question_answer117)
In Drosophila, gene for white eye mutation is also responsible for depigmentation of body parts. Thus gene that controls several phenotypes is called :
A)
Oncogene done
clear
B)
Epistatic gene done
clear
C)
Hypostatic gene done
clear
D)
Pleiotropic gene done
clear
View Solution play_arrow
-
question_answer118)
Phenylketonuria is the genetic disorder of :
A)
Trisomic condition done
clear
B)
Monosomic condition done
clear
C)
Autosomal dominant gene done
clear
D)
Autosomal recessive gene done
clear
View Solution play_arrow
-
question_answer119)
Haemophilia is a condition, where there is :
A)
No production of haemoglobin in the blood done
clear
B)
No production of melanin in the skin done
clear
C)
A failure of clotting mechanism of blood done
clear
D)
A delay in clotting of blood done
clear
View Solution play_arrow
-
question_answer120)
When the chromosome number of a given organism has one additional chromosome in one of the homologous pairs, the condition is known as
A)
Trisomy done
clear
B)
Monosomy done
clear
C)
Polyploidy done
clear
D)
Nullisomy done
clear
View Solution play_arrow
-
question_answer121)
In a skip generation inheritance of colour-blindness trait from a colour-blind man is passed on to :
A)
Daughter done
clear
B)
Son done
clear
C)
Grand daughter done
clear
D)
Grand son done
clear
View Solution play_arrow
-
question_answer122)
A medico-legal case of accidental interchange between two babies in a hospital, the baby of the blood group 'A' could not be rightly given to couple with :
A)
Husband of 'O' group and wife of 'AB' group done
clear
B)
Husband of 'A' group and wife of 'B' group done
clear
C)
Husband of 'B' group and wife of 'O' group done
clear
D)
Husband of 'AB' group and wife of 'A' group done
clear
View Solution play_arrow
-
question_answer123)
Genes present is cytoplasm of eukaryotic cells are found in :
A)
Mitochondria and inherited via egg cytoplasm done
clear
B)
Lysosomes and peroxisomes done
clear
C)
Golgi bodies and smooth endoplasmic reticulum done
clear
D)
Plastids and inherited via male gamete done
clear
View Solution play_arrow
-
question_answer124)
Action of ultraviolet rays on DNA is :
A)
Induction of thymidine done
clear
B)
Deletion of base pair done
clear
C)
Addition of base pair done
clear
D)
Methylation of base pair done
clear
View Solution play_arrow
-
question_answer125)
In Klinefelter's syndrome, the sex chromosome complement is :
A)
22A + XXY done
clear
B)
22 A + XO done
clear
C)
22 A + XY done
clear
D)
22 A + XX done
clear
View Solution play_arrow
-
question_answer126)
The recessive genes located on X-chromosome in humans are always :
A)
Lethal in male and female done
clear
B)
Sub-lethal in male and female done
clear
C)
Expressed in males done
clear
D)
Expressed in females done
clear
View Solution play_arrow
-
question_answer127)
After a mutation at a genetic locus, the character of an organism changes due to the change in :
A)
Protein structure done
clear
B)
DNA replication done
clear
C)
Enzyme pattern done
clear
D)
RNA transcription pattern done
clear
View Solution play_arrow
-
question_answer128)
A man and a woman, who do not show any apparent signs of certain inherited disease, have seven children (2 daughters and 5 sons). Three of the sons suffer from the given disease but none of the daughters are affected. Which of the following mode of inheritance, do you suggest for the disease?
A)
Autosomal dominant done
clear
B)
Sex-linked dominant done
clear
C)
Sex-limited recessive done
clear
D)
Sex-linked recessive done
clear
View Solution play_arrow
-
question_answer129)
A woman with normal vision, but whose father was colour-blind, marries a colour-blind man. Suppose that the fourth child of this couple was a boy. This boy :
A)
Must have normal colour vision done
clear
B)
Will be partially colour-blind since he is heterozygous for the colour-blind mutant allele done
clear
C)
Must be colour-blind done
clear
D)
May be colour-blind or may be of normal vision done
clear
View Solution play_arrow
-
question_answer130)
Haemophilia is more commonly seen in human males than in human females because :
A)
This disease is due to an X-linked dominant mutation done
clear
B)
A greater proportion of girls die in infancy done
clear
C)
This disease is due to X-linked recessive mutation done
clear
D)
This disease is due to Y-linked recessive mutation done
clear
View Solution play_arrow
-
question_answer131)
A woman with 47 chromosomes due to three copies of chromosome 21 is characterized by:
A)
Down syndrome done
clear
B)
Triploidy done
clear
C)
Turner syndrome done
clear
D)
Super femaleness done
clear
View Solution play_arrow
-
question_answer132)
Barr body of a mammal represents :
A)
All heterochromatin in female cells done
clear
B)
All heterochromatin in male and female cells done
clear
C)
The Y chromosome in the somatic cells of male done
clear
D)
One of the two X-chromosomes in somatic cells of female done
clear
View Solution play_arrow
-
question_answer133)
Genetic counsellors can identify heterozygous individuals by :
A)
Height of an individuals done
clear
B)
Colour of an individuals done
clear
C)
Screening procedures done
clear
D)
Weight of an individual done
clear
View Solution play_arrow
-
question_answer134)
A marriage between normal visioned man and colour-blind woman will produce, which of the following type of offspring?
A)
Normal sons and carrier daughters done
clear
B)
Colour-blind sons and carrier daughters done
clear
C)
Colour-blind sons and 50% carrier daughters done
clear
D)
50% colour-blind sons and 50% carrier daughters done
clear
View Solution play_arrow
-
question_answer135)
Linkage group in Escherichia coli is/are :
A)
4 done
clear
B)
2 done
clear
C)
1 done
clear
D)
5 done
clear
View Solution play_arrow
-
question_answer136)
Down's syndrome is caused by an extra copy of chromosome number 21. What percentage of offspring produced by an affected mother and a normal father would be affected by this disorder?
A)
50% done
clear
B)
25% done
clear
C)
100% done
clear
D)
75% done
clear
View Solution play_arrow
-
question_answer137)
Grain colour in wheat is determined by three pairs of polygenes. Following the cross AABBCC (dark colour) \[\times \] aabbcc (light colour), in \[{{F}_{2}}\] generation what proportion of the progeny is likely to resemble either parent?
A)
Half done
clear
B)
Less than 5 percent done
clear
C)
One third done
clear
D)
None of the above done
clear
View Solution play_arrow
-
question_answer138)
Complete linkage is observed in :
A)
Male Drosophila sp. done
clear
B)
Female Drosophila sp. done
clear
C)
Female silkworm done
clear
D)
Female rhesus monkey done
clear
View Solution play_arrow
-
question_answer139)
Mutations that arise suddenly in nature are called :
A)
Chromosomal mutations done
clear
B)
Induced mutations done
clear
C)
Gene mutations done
clear
D)
Spontaneous mutations done
clear
View Solution play_arrow
-
question_answer140)
Occurrence of cell containing multiples of 2n genomes in diploid organisms is known as :
A)
Aneuploidy done
clear
B)
Alloploidy done
clear
C)
Amphiploidy done
clear
D)
Endopolyploidy done
clear
View Solution play_arrow
-
question_answer141)
Skin colour in man is determined by three pairs of polygenes. Following the cross AABBCC (dark colour) \[\times \] aabbcc (light colour), in \[{{F}_{2}}\] generation what proportion of the progeny is likely to resemble either parent?
A)
50% done
clear
B)
3% done
clear
C)
25% done
clear
D)
75% done
clear
View Solution play_arrow
-
question_answer142)
Which of the following pair of features is a good example of polygenic inheritance?
A)
Human height and skin colour done
clear
B)
ABO blood group in humans and flower colour of Mirabilis jalapa done
clear
C)
Hair pigment of mouse and tongue rolling in humans done
clear
D)
Human eye colour and sickle cell anaemia done
clear
View Solution play_arrow
-
question_answer143)
The gene which controls many characters is called :
A)
Codominant gene done
clear
B)
Polygene done
clear
C)
Pleiotropic gene done
clear
D)
Multiple gene done
clear
View Solution play_arrow
-
question_answer144)
Sickle cell anaemia is :
A)
Autosomal dominant inheritance done
clear
B)
X-linked recessive inheritance done
clear
C)
Autosomal recessive inheritance done
clear
D)
X-linked dominant inheritance done
clear
View Solution play_arrow
-
question_answer145)
Polyploidy can be produced artificially by :
A)
Colchicine done
clear
B)
Inbreeding done
clear
C)
Line breeding done
clear
D)
Self-pollination done
clear
View Solution play_arrow
-
question_answer146)
Karyotype is :
A)
Chromosome complement which is specific for each species of living organism done
clear
B)
All organisms possessing same type of chromosomes done
clear
C)
Division of nucleus done
clear
D)
One of the above done
clear
View Solution play_arrow
-
question_answer147)
Identify the wrong statements:
A)
In male grasshoppers 50 % of the sperms have no sex chromosome done
clear
B)
Usually female birds produce two types of gametes based on sex chromosomes done
clear
C)
The human males have one of their sex chromosomes much shorter than the other done
clear
D)
In domesticated fowls the sex of the progeny depends on the type of sperm that fertilizes the egg done
clear
View Solution play_arrow
-
question_answer148)
Gynaecomastia is a common feature seen in:
A)
Down's syndrome done
clear
B)
Turner's syndrome done
clear
C)
PKU done
clear
D)
Klinefelter's syndrome done
clear
View Solution play_arrow
-
question_answer149)
The graphical representation to calculate the probability of all possible genotypes of offspring in a genetic cross is called :
A)
Pedigree analysis done
clear
B)
Karyotype done
clear
C)
Punnett square done
clear
D)
Chromosome map done
clear
View Solution play_arrow
-
question_answer150)
Chromosome is made up of :
A)
DNA + pectin done
clear
B)
RNA + DNA done
clear
C)
DNA + histone done
clear
D)
Only histone done
clear
View Solution play_arrow
-
question_answer151)
What is shown in the following figure of human pedigrees? |
|
A)
Autosomal dominant trait like Sickle - cell anaemia done
clear
B)
Allosomal recessive trait like Sickle - cell anaemia done
clear
C)
Autosomal recessive trait like colour blindness done
clear
D)
Autosomal recessive trait like Sickle - cell anaemia done
clear
View Solution play_arrow
-
question_answer152)
In honeybee haploid stage develop into
A)
Male caste done
clear
B)
Female caste done
clear
C)
Neutral caste done
clear
D)
All of these done
clear
View Solution play_arrow
-
question_answer153)
The number of linkage group(s) present in man is :
A)
One done
clear
B)
Two done
clear
C)
Twenty-three done
clear
D)
Seven done
clear
View Solution play_arrow
-
question_answer154)
The major cause of evolution of genes and protein is :
A)
Point mutation done
clear
B)
Chromosomal aberration done
clear
C)
Sexual reproduction done
clear
D)
Gene duplication and divergence done
clear
View Solution play_arrow
-
question_answer155)
Due to nondisjunction of chromosomes during spermatogenesis, sperms carry both sex chromosomes (22A + XY) and some sperms do not carry any sex chromosome (22A + X). If these sperms fertilize normal eggs (22A + X), what types of genetic disorders appear among the offsprings?
A)
Turner's syndrome and Klinefelter's syndrome done
clear
B)
Down's syndrome and Klinefelter's syndroos done
clear
C)
Down's syndrome and Turner's syndrome done
clear
D)
Down's syndrome and cri-du-chat syndrora done
clear
View Solution play_arrow
-
question_answer156)
Which genetic disorder is caused due to the presence of an additional copy of X-chromosome (A Karyotype of 44, XXY)?
A)
Klinefelter's syndrome done
clear
B)
Down's syndrome done
clear
C)
Turner syndrome done
clear
D)
Edward's syndrome done
clear
View Solution play_arrow
-
question_answer157)
Multiple phenotype is seen in:
A)
dominance relationship done
clear
B)
paniculate inheritance done
clear
C)
monogenic inheritance done
clear
D)
polygenic inheritance done
clear
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question_answer158)
Cystic Fibrosis disease in human being is due to
A)
chromosome 5 done
clear
B)
chromosome 6 done
clear
C)
chromosome 7 done
clear
D)
chromosome 8 done
clear
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question_answer159)
In XO type of sex determination
A)
females produce two different types of gametes done
clear
B)
males produce two different types of gametes done
clear
C)
females produce gametes with Y chromosomes done
clear
D)
males produce single type of gametes done
clear
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question_answer160)
Who used the frequency of recombination between gene pairs on the same chromosome as a measure of the distance between genes and mapped their position on the chromosome?
A)
Gregor Mendel done
clear
B)
Correns done
clear
C)
Tschermark done
clear
D)
Alfred Sturtevant done
clear
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question_answer161)
Sickle cell anaemia is caused by the substitution of
A)
valine by glutamic acid at sixth position of alpha chain of haemoglobin. done
clear
B)
valine by glutamic acid at sixth position of beta chain of haemoglobin. done
clear
C)
glutamic acid by valine at sixth position of alpha chain of haemoglobin. done
clear
D)
glutamic acid by valine at sixth position of beta chain of haemoglobin done
clear
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question_answer162)
Which following pair of diseases is caused by two genes located on human X-Chromosome?
A)
Colour blindness and phenylketonuria. done
clear
B)
Colour blindness and haemophilia. done
clear
C)
Colour blindness and albinism. done
clear
D)
Colour blindness and hypertrichosis. done
clear
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question_answer163)
XX-XO type sex determination is recorded in
A)
Grasshopper done
clear
B)
Drosophila done
clear
C)
Frog done
clear
D)
Earthworm done
clear
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question_answer164)
In XO types of sex determination
A)
females produce two different types of gametes done
clear
B)
Males produce two different types of gametes done
clear
C)
females produce gametes with Y chromosomes done
clear
D)
males produce single type of gametes done
clear
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question_answer165)
The behaviour of the chromosomes was parallel to the behaviour of genes during meiosis was noted by
A)
Correns done
clear
B)
Tschermark done
clear
C)
Sutton and Boveri done
clear
D)
de Vries done
clear
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question_answer166)
Genes with multiple phenotypic effects are known as
A)
hypostatic genes done
clear
B)
duplicate genes done
clear
C)
pleiotropic genes done
clear
D)
complementary genes done
clear
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question_answer167)
In case of incomplete linkage, the parental combinations obtained in \[{{F}_{2}}\], generation are
A)
100% done
clear
B)
more than 50% done
clear
C)
25% done
clear
D)
less than 50% done
clear
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question_answer168)
Loss or gain of one more complete set of chromosomes along with the diploid complement is known as
A)
aneuploidy done
clear
B)
euploidy done
clear
C)
reverse tandem duplication done
clear
D)
substitution done
clear
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question_answer169)
The traits which are expressed in only a particular sex through their genes occurs in the opposite sex too are known as
A)
sex linked trait done
clear
B)
sex influence trait done
clear
C)
sex limited traits done
clear
D)
sex affected traits done
clear
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question_answer170)
Heterogamety is the term where an individual produces two types of gametes. The most appropriate answer is
A)
Male Drosophila fly done
clear
B)
Female Drosophila fly done
clear
C)
Female bird done
clear
D)
Both [a] and [c] done
clear
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question_answer171)
In our society women are blamed for producing female children. Choose the correct answer for the sex-determination in humans.
A)
Due to some defect like aspermia in man done
clear
B)
Due to the genetic make up of the particular sperm which fertilizes the egg done
clear
C)
Due to the genetic make up of the egg done
clear
D)
Due to some defect in the women. done
clear
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question_answer172)
Genetic variation in a population arises due to
A)
recombination only done
clear
B)
mutation as well as recombination done
clear
C)
reproductive isolation and selection done
clear
D)
mutations only done
clear
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question_answer173)
Which one is the incorrect statement with regard to the importance of pedigree analysis?
A)
It confirms that DNA is the carrier genetic information done
clear
B)
It helps to understand whether the trait in question is dominant or recessive. done
clear
C)
It confirms that the trait is linked to one of the autosomes. done
clear
D)
It helps to trace the inheritance of a specific trait. done
clear
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question_answer174)
A colour-blind man marries the daughter of another colour-blind man whose wife has a normal genotype for colour vision. In their progeny
A)
all the children would be colour-blind done
clear
B)
all their sons are colour-blind done
clear
C)
none of the daughters would be colour-blind done
clear
D)
half of their sons and half of their daughters would be colour-blind. done
clear
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question_answer175)
Klinefelter's syndrome in human is an example of
A)
Auto polyploidy done
clear
B)
Allopolyploidy done
clear
C)
Diploidy done
clear
D)
Aneuploidy done
clear
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question_answer176)
A person affected with phenylketonuria, lacks an enzyme that converts the amino acid phenylalanininto
A)
valine done
clear
B)
proline done
clear
C)
histidine done
clear
D)
tyrosine done
clear
View Solution play_arrow
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question_answer177)
In sickle cell anemia, the sequence of amino acids from the first to the seventh position of the p-chain of haemoglobin S(HbS) is
A)
His, Leu, Thr, Pro, Glu, Val, Val done
clear
B)
Val, His, Leu, Thr, Pro, Glu, Glu done
clear
C)
Thr, His, Pro, Val, Pro, Val, Glu done
clear
D)
Val, His, Leu, Thr, Pro, Val, Glu done
clear
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question_answer178)
Statement-A: For a particular character in an individual, each gamete gets only one allele. |
Statement-B: Chromatids of a chromosome split (separate) and move towards opposite poles during anaphase of mitosis. |
A)
Statement A is correct and statement B is wrong. done
clear
B)
Both the statements are correct and B is the reason for A. done
clear
C)
Statement B is correct and statement A is wrong. done
clear
D)
Both the statements are correct and B is not the reason for A. done
clear
View Solution play_arrow
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question_answer179)
Sickle cell anaemia is caused due to the substitution of
A)
valine at the 6th position of beta globin chain by glutamine done
clear
B)
valine at the 6th position of alpha globin chain by glutamic acid done
clear
C)
glycine at the 6th position of alpha globin chain by glutamic acid done
clear
D)
glutamic acid at the 6th position of beta globin chain by valine done
clear
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question_answer180)
Anish is having colour blindness and married to Sheela, who is not colour-blind. What is the chance that their son will have the disease?
A)
100% done
clear
B)
50% done
clear
C)
25% done
clear
D)
0% done
clear
View Solution play_arrow
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question_answer181)
The frequency of crossing over occurring between two genes located on the same chromosome depends on
A)
length of the chromosome done
clear
B)
position of the centromere done
clear
C)
activities of two genes done
clear
D)
distance between two genes done
clear
View Solution play_arrow
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question_answer182)
The enzyme involved in the crossing over between two homologous chromosomes is
A)
nuclease done
clear
B)
RNA polymerase done
clear
C)
recombinase done
clear
D)
DNA polymerase done
clear
View Solution play_arrow
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question_answer183)
A couple, both carriers for the gene sickle cell anaemia planning to get married, wants to know the chances of having anaemic progeny?
A)
100% done
clear
B)
75% done
clear
C)
50% done
clear
D)
25% done
clear
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question_answer184)
The total number of types of gametes produced in across between a negro and albino parent is
A)
64 done
clear
B)
16 done
clear
C)
08 done
clear
D)
04 done
clear
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question_answer185)
Which of the following is correct match?
A)
B)
C)
D)
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question_answer186)
Sex determination by chromosomal difference in man and Drosophila is by mechanism called
A)
XX-XY done
clear
B)
XX-XO done
clear
C)
ZZ-ZW done
clear
D)
Both [a] and [b] done
clear
View Solution play_arrow
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question_answer187)
Which of the following set of syndromes show 47 chromosomes in their genetic make up?
A)
Down's syndrome, Patau's syndrome, Edward's syndrome done
clear
B)
Turner's syndrome, Edward's syndrome, Klinefelter's syndrome done
clear
C)
Klinefelter's syndrome. Turner's syndrome, Edward's syndrome done
clear
D)
All the above done
clear
View Solution play_arrow
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question_answer188)
In order to lessen the suffering of phenylketonurics their diet should have
A)
no phenylalanine and no tyrosine done
clear
B)
low phenylalanine and normal requirement of tyrosine done
clear
C)
normal recommended amount of phenylalanine done
clear
D)
normal recommended amount of both phenylalanine and tyrosine done
clear
View Solution play_arrow
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question_answer189)
Drosophila flies with XXY genotype are females, but human beings with such genotype are abnormal males. It shows that :
A)
Y-chromosome is essential for sex determination in Drosophila done
clear
B)
Y-chromosome in female determining in Drosophila done
clear
C)
Y-chromosome is male determining in human beings done
clear
D)
Y-chromosome has no role in sex determination either in Drosophila or in human beings done
clear
View Solution play_arrow
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question_answer190)
Linkage groups : |
1. Have genes, which were linked together in a single chromosome |
2. Show independent assortment |
3. Do not show independent assortment |
4. In prokaryotes are more than one |
A)
1, 2 and 3 are correct done
clear
B)
1 and 2 are correct done
clear
C)
2 and 4 are correct done
clear
D)
1 and 3 are correct done
clear
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question_answer191)
Which of the following statements about colour blindness is correct?
A)
2% men are red colour blind, 6% are green colour blind done
clear
B)
6% men are red colour blind, 2% are green colour blind done
clear
C)
10% men are red colour blind, 5% are green colour blind done
clear
D)
5% men are red colour blind, 10% are green colour blind done
clear
View Solution play_arrow
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question_answer192)
Choose the wrong statement.
A)
In grasshoppers, besides autosomes males have only one X-chromosome, whereas females have a pair of X-chromosomes. done
clear
B)
In XY type of sex determination, both males and females have same number of chromosomes. done
clear
C)
In Drosophila, males have one X and one Y chromosome, whereas females have a pair of X- chromosomes besides autosomes done
clear
D)
In insects with XO type of sex determination, all sperms bear X-chromosome besides autosomes done
clear
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question_answer193)
Which one of the following is an example of poly genie inheritance?
A)
Flower colour in Mirabilis jalapa done
clear
B)
Production of male honey bee done
clear
C)
Pod shape in garden pea done
clear
D)
Skin colour in humans done
clear
View Solution play_arrow
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question_answer194)
Identify a Mendelian disorder from the following :
A)
Down's syndrome done
clear
B)
Turner's syndrome done
clear
C)
Phenylketonuria done
clear
D)
Kline feller's syndrome done
clear
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question_answer195)
A man, whose father is colour blind, marries a lady who is daughter of a colour-blind man. Their off springs will be
A)
all normal done
clear
B)
all colour blinds done
clear
C)
all sons colour blind done
clear
D)
some sons colour blind and some normal done
clear
View Solution play_arrow