A pleiotropic gene:

1. Is expressed only in primitive plants
2. Is a gene that evolved during Pliocene
3. Controls a trait only in combination with another gene
4. Controls multiple traits in an individual 

Subtopic:  Polygenic Inheritance & Pleiotropy |
 90%
From NCERT
NEET - 2015
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The movement of a gene from one linkage group to another is called:

1. inversion
2. duplication
3. translocation
4. crossing over
Subtopic:  Understanding Linkage |
 76%
NEET - 2015
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Fruit colour in squash is an example of:

1. Recessive epistasis

2. Dominant epistasis

3. Complementary genes

4. Inhibitory genes

Subtopic:  Epistasis |
 63%
AIPMT - 2014
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If both parents are carriers for thalassemia, which is an autosomal recessive disorder, what are the chances of pregnancy resulting in an affected child?
1. 50% 2. 25 %
3. 100% 4. no chance
Subtopic:  Mendelian Disorders: Thalassemia |
 56%
From NCERT
AIPMT - 2013
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A man whose father was colour blind marries a woman who had a colour blind mother and a normal father. What percentage of male children of this couple will be colour blind?

1. 25%

2. 0%

3. 50%

4. 75%

Subtopic:  Sex Linked Recessive Inheritance |
 62%
From NCERT
AIPMT - 2014
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Which one of the following conditions correctly describes the manner of determining the sex in the given example?
 
1. XO type of sex chromosomes determines male sex in grasshopper
2. XO condition in humans as found in Turner syndrome, determines female sex
3. Homozygous sex chromosomes (XX) produce males in Drosophila
4. Homozygous sex chromosomes (ZZ) determine the female sex in birds.
Subtopic:  Sex Determination |
 80%
From NCERT
AIPMT - 2011
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Sickle cell anaemia is:

1. an autosomal linked dominant trait
2. caused by substitution of valine by glutamic acid
in the globin chain of haemoglobin
3. caused by a change in base pair of DNA
4. characterized by elongated sickle like RBCs with
a nucleus

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 53%
From NCERT
AIPMT - 2009
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In hexaploid wheat, the haploid (n) ar basic (x) numbers of chromosomes are:

1. n=7 and x=21

2. n=21 and x=21

3. n=21 and x=14

4. n=21 and x=7

Subtopic:  Non - Disjunction & Aneuploidy |
AIPMT - 2007
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Inheritance of skin colour in humans is an example of:

1. chromosomal aberration

2. point mutation

3. polygenic inheritance

4. codominance

Subtopic:  Polygenic Inheritance & Pleiotropy |
 91%
From NCERT
AIPMT - 2007
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Two genes R and Y are located very close on the chromosomal linkage map of the maize plant. When RRYY and rryy genotypes are hybridized, then F2 segregation will show:

1. higher number of the recombinant types

2. segregation in the expected 9:3:3:1 ratio

3. segregation in a 3:1 ratio

4. higher number of the parental types

Subtopic:  Dihybrid Cross Analysis | Dihybrid Cross: Details |
 61%
From NCERT
AIPMT - 2007
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