Suppose a gene has seven alleles. What would be the number of alleles in an individual at any instant?

(1) 1

(2) 7

(3) 2

(4) 3

Subtopic:  Dominance Deviation from Mendel: 2 |
 59%
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In case of starch synthesis in pea seeds [controlled by B gene], BB homozygotes produce large and round starch grains; bb homozygotes produce smaller and wrinkled starch grains and Heterozygotes produce round seeds of intermediate size. What can be inferred from this observation?

(1) The gene B mutates at a faster rate.

(2) The gene B is easily influenced by the environment

(3) Dominance is not an autonomous feature of a gene or the product that it has information for

(4) Some genes do not follow the law of segregation

Subtopic:  Dominance Deviation from Mendel: 1 |
 83%
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When Mendel self hybridized F1 progeny of a dihybrid cross between pure Yellow Round seeded plants and Green Wrinkled plants, he observed that yellow and green colour segregated in a ratio of:

(1) 1 : 1

(2) 3 : 1

(3) 9 : 3 : 3 : 1

(4) 1 : 2 : 1

Subtopic:  Dihybrid Cross: Details |
 50%
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In 1900 Mendel’s work was rediscovered by:

1. Korana, Nirenberg and Mathei

2. De Vries, Correns and von Tschermak

3. Avery, McCleod and McCarty

4. Watson, Crick and Wilkins

Subtopic:  Monohybrid Cross: 1 |
 91%
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Genes tightly linked on the same chromosome show:

(1) Very high recombination

(2) Independent assortment

(3) Very low recombination

(4) 50 % recombination

Subtopic:  Linkage |
 88%
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In humans, the mechanism of sex determination is:

(1) XX – XY; male heterogamety

(2) XX – XY; female heterogamety

(3) XX – XO; male heterogamety

(4) XX – XO; female heterogamety

Subtopic:  Sex Determination |
 93%
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A couple has a daughter. What is the probability that their next child will be a daughter?

(1) 0 %

(2) 25 %

(3) 50 %

(4) 100 %

Subtopic:  Sex Determination |
 92%
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Thalesemia is inherited as a/an ____________ condition.

(1) Autosomal recessive

(2) Autosomal dominant

(3) Sex linked recessive

(4) Sexlinked dominant

Subtopic:  Mendelian Disorders: Thalassemia |
 86%
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The point mutation in sickle cell anaemia leads to a change in codon. Identify the correct change:

(1) UGA to UAA

(2) GUG to GAG

(3) GAG to GUG

(4) UAA to UGA

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 83%
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In sickle cell anaemia, the mutant haemoglobin molecule undergoes

(1) Polymerisation under low oxygen tension causing that changes the shape of the RBC to sickle like structure

(2) Depolymerisation under low oxygen tension causing that changes the shape of the RBC to sickle like structure

(3) Denaturation under high oxygen tension causing that changes the shape of the RBC to sickle like structure

(4) Denaturation

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 79%
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