Which one of the following symbols and its representation, used in the human pedigree analysis is correct?

1. = Mating between relatives
2.     = Unaffected male
3.     = Unaffected female
4.     = male affected

Subtopic:  Pedigree Analysis: Basics |
 86%
AIPMT - 2010
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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 |
 52%
From NCERT
AIPMT - 2009
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Point mutation involves:

1. insertion

2. change in single base pair

3. duplication 

4. deletion

Subtopic:  Mutation |
 92%
From NCERT
AIPMT - 2009
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Study the pedigree chart given below:



What does it show?

1. Inheritance of a sex-linked inborn error of metabolism
2. Inheritance of a condition like phenylketonuria as an
autosomal recessive trait
3. The pedigree chart is wrong as this is not possible
4. Inheritance of a recessive sex-linked disease like
haemophilia

Subtopic:  Pedigree Analysis: Problem Solving | Mendelian Disorders |
 77%
From NCERT
AIPMT - 2009
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Select the incorrect statement from the following:

1. linkage is an exception to the principle of
independent assortment in heredity
2. galactosemia is an inborn error of metabolism
3. small population size result in random genetic
drift in a population
4. baldness is a sex-limited trait

Subtopic:  Sex Linked Inheritance: Introduction |
AIPMT - 2009
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A human male produces sperms with the genotypes AB, Ab, aB and ab pertaining to two diallelic characters in equal proportions. What is the corresponding genotype of this person?

1. AaBb

2. AaBB

3. AABb

4. AABB

Subtopic:  Dihybrid Cross: Details |
 80%
AIPMT - 2007
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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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Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage?
1. Klinefelter's syndrome-44 autosomes + XXY
2. Colourblindness – Y-linked
3. Erythroblastosis foetalis-- X-linked
4. Down syndrome--44 autosomes + XO
Subtopic:  Sex Aneuploidy - Turner & Klinefelter Syndrome |
 85%
From NCERT
AIPMT - 2008
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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 |
 92%
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 |
 60%
From NCERT
AIPMT - 2007
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