Which of the following is not an autosomal genetic disorder ?

(1) Sickle-cell anaemia

(2) Cystic fibrosis

(3) Haemophilia

(4) Huntington's disease

Subtopic:  Mendelian Disorders |
 74%
From NCERT
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Study the pedigree chart of a family showing the inheritance of myotonic dystrophy.

 

The trait under study is 

1. dominant X-linked

2. recessive X-linked

3. autosomal dominant

4. recessive Y-linked.

Subtopic:  Pedigree Analysis: Problem Solving |
 74%
From NCERT
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The ratio in a dihybrid test cross between two individuals is given by

(1) 2:1

(2) 1:2:1

(3) 3:1

(4) 1:1:1:1

Subtopic:  Dihybrid Cross Analysis |
 68%
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A point mutation comprising the substitution of a purine by pyrimidine is called

(1) transition

(2) translocation

(3) deletion

(4) transversion

Subtopic:  Recombination Gene Mapping |
 53%
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Pure line breed refers to

(1) heterozygosity only

(2) heterogyzosity and linkage

(3) homozygosity only

(4) homozygosity and self assortment.

Subtopic:  Monohybrid Cross: 1 |
 62%
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One of the genes present exclusively on the X-chromosome in humans is concerned with

1. baldness

2. red-green colour blindness

3. facial hair/moustaches in males

4. night blindness

Subtopic:  Sex Linked Inheritance: Introduction |
 75%
From NCERT
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Given below is a pedigree chart of a family with five children. It shows the inheritance of attached ear-lobes as opposed to the free ones. The squares represent the male individuals and circles the females individuals. Which one of the foloowing conclusions drawn is correct?

(1) The parents are homozygous recessive.

(2) The trait is Y-linked.

(3) The parents are homozygous dominant.

(4) The parents are heterozygous.

Subtopic:  Pedigree Analysis: Problem Solving |
 63%
AIIMS - 2004
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How many different types of gametes can be formed by F1 progeny, resulting from the following cross:

AA BB CC X aa bb cc

(1) 3

(2) 8

(3) 27

(4) 64

Subtopic:  Dihybrid Cross: Details |
 65%
AIIMS - 2004
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Given below is a pedigree chart showing the inheritance of a certain sex-liniked trait in humans. 

The Trait traced in the above pedigree chart is 

(1) dominant X-linked 

(2) recessive X-linked

(3) dominant Y-linked

(4) recessive Y-linked

Subtopic:  Pedigree Analysis: Problem Solving |
 65%
AIIMS - 2005
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The "cri-du-chat" syndrome is caused by change in chromosome structure invloving

(1) deletion

(2) duplication

(3) inversion

(4) translocation

Subtopic:  Recombination Gene Mapping |
 66%
AIIMS - 2005
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