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प्रश्न
Match the column-I with column-II and re-write the matching pairs.
| Column-I | Column-II |
| 1. 21 trisomy | a. Turner’s syndrome |
| 2. X-monosomy | b. Klinefelter’s syndrome |
| 3. Holandric traits | c. Down's syndrome |
| 4. Feminized male | d. Hypertrichosis |
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उत्तर
| Column-I | Column-II |
| 1. 21 trisomy | c. Down's syndrome |
| 2. X-monosomy | a. Turner’s syndrome |
| 3. Holandric traits | d. Hypertrichosis |
| 4. Feminized male | b. Klinefelter’s syndrome |
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संबंधित प्रश्न
Give an example of an autosomal recessive trait in humans. Explain its pattern of inheritance with the help of a cross.
Give an example of a human disorder that is caused due to a single gene mutation.
Answer the following question.
Both Haemophilia and Thalessemia are blood-related disorders in humans. Write their causes and the difference between the two. Name the category of genetic disorder they both come under.
Very Short Answer Question.
Give an example of a chromosomal disorder caused due to nondisjunction of autosomes.
Give reasons for the development of Turner’s syndrome and also mention its symptoms.
A woman with albinic father marries an albinic man. The proportion of her progeny is ______.
A person with 47 chromosomes due to an additional Y-chromosome suffers from a condition called ______.
Which of the following is called as Royal disease?
Fused ear lobes appear in the progeny due to an autosomal recessive gene. Work out the genotypes of number in the given pedigree.
Give the genotype of Klinefelter’s syndrome.
