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Which of the following conditions is caused by mutations that involves the entire chromosome rather than a gene?

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Important Questions on Principles of Inheritance and Variation

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Broad palm with single palm crease is visible in a person suffering from- 
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Which of the following statements are correct about Klinefelter's Syndrome?

A. This disorder was first described by Langdon Down (1866).

B. Such an individual has overall masculine development. However, the feminine development is also expressed.

C. The affected individual is short statured.

D. Physical, psychomotor and mental development is retarded.

E. Such individuals are sterile.

Choose the correct answer from the options given below: 

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A colourblind man marries a woman with normal sight who has no history of colour blindness in her family. What is the probability of their sons being colourblind?
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Pick out the correct statements:
(i) Haemophilia is a sex-linked recessive disease.
(ii) Down's syndrome is due to aneuploidy.
(iii) Phenylketonuria is an autosomal recessive gene disorder.
(iv) Sickle cell anaemia is an X-linked recessive gene disorder.
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Match the Column- I with Column - II

  Column - I   Column - II
i Autosomal trisomy p Turner's Syndrome
ii Allosomal trisomy q Mendelian disorder
iii Allosomal Monosomy r Klinefelter's Syndrome
iv Cystic fibrosis s Down's Syndrome
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People suffering from albinism cannot synthesize:
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Conditions of a karyotype 2n±1 and 2n±2 are called
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Which one of the following genotype does NOT represent aneuploidy in human being?
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In the following human pedigree, the filled symbols represents the affected individuals. Identify the type of given pedigree.


Question Image
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A disease caused by an autosomal primary non-disjunction is
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If a colour-blind man marries a woman who is homozygous for normal colour vision, the probability of their son being colour-blind is
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Which of the following most appropriately describes haemophilia?
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Match the human disorders shown in Group I with the biochemical processes in Group II. Choose the correct combination.
 
Group I Group II
P. Phenylketonuria i. Melanin synthesis
Q. Albinism ii. Conversion of Phenylalanine to Tyrosine
R. Homocystinuria iii. Tyrosine degradation
S. Argininemia iv. Methionine metabolism
  v. Urea Synthesis
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A woman heterozygous for colour blindness marries a colour-blind man. What would be the ratios of carrier daughters, colour-blind daughters, normal sons, and colour-blind sons in the F1 generation?

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Children suffering from phenylketonuria are given food low in phenylalanine and supplemented with tyrosine. This is because they
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How many number of barr body will be present in female suffering from Turner's syndrome?
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The genetic disorder in which an individual has an overall masculine development, gynaecomastia and is sterile:
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An abnormal human baby with 'XXX' sex chromosomes was born due to: