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NEET BIOLOGYPrinciples of Inheritance and VariationMedium

Question

In the following human pedigree, the filled symbols represent the affected individuals. Identify the type of given pedigree:

A

Autosomal dominant

B

X-linked recessive

C

Autosomal recessive

D

X-linked dominant

Step-by-Step Solution

, pedigree analysis is a strong tool to trace the inheritance of specific traits. The text describes two representative pedigrees in Figure 4.14: (a) Autosomal dominant trait (e.g., Myotonic dystrophy), where the trait appears in every generation and affected individuals have affected parents; and (b) Autosomal recessive trait (e.g., Sickle-cell anaemia), where the trait can appear in the progeny of unaffected carrier parents . While the image is not provided here, standard questions with this phrasing typically refer to the Autosomal Dominant chart showing Myotonic dystrophy.

Exam Context & Concepts Covered

This question aligns with the NEET BIOLOGY syllabus, specifically targeting concepts from Principles of Inheritance and Variation. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.

BIOLOGYPrinciples of Inheritance and Variationfollowingpedigreefilledsymbolsrepresent

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Mental retardation in man occurs due to:

A.Loss of one X chromosome
B.Addition of one X chromosome
C.Slight growth in Y
D.Overgrowth in Y
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A.(A) is True but (R) is False.
B.(A) is False but (R) is True.
C.Both (A) and (R) are True and (R) is the correct explanation of (A).
D.Both (A) and (R) are True but (R) is not the correct explanation of (A).
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A certain plant homozygous for yellow seeds and red flowers was crossed with a plant homozygous for green seeds and white flowers. The F1 plants had yellow seeds and pink flowers. The F1 plants were selfed to get F2 progeny. Assuming independent assortment of the two characters, how many phenotypic categories are expected for these characters in the F2 generation?

A.9
B.16
C.4
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In Drosophila the XXY condition leads to femaleness whereas in human beings the same condition leads to Klinefelter's syndrome in males. It proves:

A.In human beings, the Y chromosome is active in sex determination.
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C.In Drosophila Y-chromosome decides femaleness.
D.The Y chromosome of man has genes for the syndrome.
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What ratio is expected in offsprings if father is colour blind and mother's father was colour blind:

A.50% daughter – colour blind
B.All the sons are colour blind
C.All the daughters colour blind
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In a cross between a male and female, both heterozygous for sickle cell anaemia gene, what percentage of the progeny will be diseased?

A.25%
B.100%
C.50%
D.75%
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A.Baby is male
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A genetic map is one that:

A.Establishes sites of the genes on a chromosome
B.Establishes the various stages in gene evolution
C.Shows the stages during the cell division
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