Linkage map of X-chromosome of fruitfly has 66 map units with yellow body gene(y) at one end & bobbed hair (b) at the other. The recombination frequency between y and b gene would be
1. 66%
2. > 50%
3. 50%
4. 100%

Subtopic:  Linkage |
 54%
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A harmful condition which is also a potential saviour from a mosquito borne infectious disease
1. Thalassemia
2. Sickle cell anaemia
3. Leukemia
4. Pernicious anaemia

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 79%
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One of the genes present exclusively on the X-chromosome in humans is concerned with
1. Baldness
2. Red-green color blindness
3. Facial hair/moustaches in males
4. Night blindness

Subtopic:  Mendelian Disorders |
 75%
From NCERT
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Self fertilising trihybrid plants form
1.Eight different gametes and 64 different zygotes
2. Four different gametes and sixteen different zygotes
3. Eight different gametes and sixteen different zygotes
4. Eight different gametes and thirty two different zygotes

Subtopic:  Dihybrid Cross: Details |
 71%
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A normal woman whose father was colour blind is married to normal visioned man. Their sons would be
1. 75% colour blind
2. 50% colour blind
3. 100% colour blind
4. All normal.

Subtopic:  Pedigree Analysis: More Examples | Mendelian Disorders |
 81%
From NCERT
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For finding the different types of gametes produced by genotype AaBb, it should be crossed with genotype
1. AABB
2. aabb
3. AaBb
4. aaBB.

Subtopic:  Dihybrid Cross: Details |
 67%
From NCERT
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A normal couple has seven children (2 daughters and 5 sons). Three of the sons suffer from a hereditary disorder but none of the daughters is affected. Which is the inheritance type
1. Sex-limited recessive
2. Autosomal dominant
3. Sex-linked dominant
4. Sex-linked recessive.

Subtopic:  Sex Linked Recessive Inheritance |
 74%
From NCERT
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A woman with normal vision but with colorblind father marries a colorblind man. The fourth child of the couple is a boy. This boy
1. May or may not be colorblind
2. Must be colorblind
3. Must have normal vision
4. Will be partially colorblind due to being heterozygous

Subtopic:  Pedigree Analysis: Problem Solving |
 74%
From NCERT
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Phenotype of an organism is the result to
1. Mutations and linkages
2. Genotype and environment interactions
3. Cytoplasmic effects and nutrition
4. Environmental changes and sexual dimorphism.

Subtopic:  Introduction to Genetics: 1 | Introduction to Genetics: 2 |
 73%
From NCERT
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Cri-du-chat syndrome in humans is caused by
1. Trisomy of 21st chromosome
2. Loss of half of short arm of chromosome 5
3. Loss of half of long arm of chromosome 5
4. Fertilization of an XX egg by a normal Y- bearing sperm.

Subtopic:  Non - Disjunction & Aneuploidy |
 69%
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