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-$II$

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In which of the genetic disorders does an individual have an overall masculine development,gynaecomastia,and is sterile?

$21$ trisomy in humans causes

Choose the correct answer regarding the following statements:
$(i)$ Sickle-cell anaemia is controlled by three pairs of alleles.
$(ii)$ Trisomy is a chromosomal disorder.
$(iii)$ $47$ chromosomes are present in a person having Turner's syndrome.

Match Column $-I$ with Column $-II$ and select the correct option.
Column $-I$Column $-II$
$(P)$ Turner syndrome$(i)$ Sex chromosome $(2n-1)$
$(Q)$ Down syndrome$(ii)$ Sex chromosome $(2n+1)$
$(R)$ Klinefelter syndrome$(iii)$ Autosomal $(2n+1)$

In Klinefelter's syndrome,what is generally the set of sex chromosomes?

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