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 |
List I | List II | ||
A | Down’s syndrome | I | 11th chormosome |
B | α-Thalassemia | II | ‘X’ chromosome |
C | β-Thalassemia | III | 21st chromosome |
D | Klinefelter’s syndrome | IV | 16th chromosome |
List-I | List-II |
(A) Thalassemia | (I) 47, XXY |
(B) Klinefelter’s syndrome | (II) Sex-linked recessive disorder |
(C) Turner’s syndrome | (III) 45, XO |
(D) Colour blindness | (IV) Autosomal recessive disease |