KCET · BIOLOGY · STD 12 - 4. Principles of Inheritance and Variation
Three copies of chromosome - 21 in a child with Down's syndrome have been analysed using molecular biology technology to detect any possible DNA polymorphism with reference to different alleles located on chromosome - 21. Results showed that out of 3 copies, 2 of the chromosomes of the child contain the same alleles as one of the mother's alleles. Based on this when did the non-disjunction event most likely occur?
- A Paternal meiosis-I
- B Maternal meiosis-I
- C Paternal meiosis-II
- D Maternal meiosis-II
Answer & Solution
Correct Answer
(B) Maternal meiosis-I
Step-by-step Solution
Detailed explanation
(B) Maternal meiosis-I,
Down's syndrome is an autosomal aneuploidy, caused by the presence of an extra chromosome number 21. Usually non-disjunction of chromosomes takes place in meiosis-I.
Down's syndrome is an autosomal aneuploidy, caused by the presence of an extra chromosome number 21. Usually non-disjunction of chromosomes takes place in meiosis-I.
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