Match the following genetic disorders in Column I with associated typical chromosomal changes mentioned in Column II
|
Column I |
Column II |
||
|
(P) |
Klinefelter syndrome |
i) |
45, XO |
|
(Q) |
Down syndrome |
ii) |
5p minus |
|
(R) |
Turner syndrome |
iii) |
47, XXY |
|
(S) |
Cri du chat syndrome |
iv) |
Trisomy 21 |
1
P-(iv), Q-(iii), R-(ii), S-(i)
2
P-(iv), Q-(ii), R-(i), S-(iii)
3
P-(iii), Q-(iv), R-(ii), S-(i)
4
P-(iii), Q-(iv), R-(i), S-(ii)