184736
Match the human genetic disorder with the causative abnormal chromosome
| A. | Sickle cell anaemia | 1. | Sex linked (X
chromosome) |
| :--- | :--- | :--- | :--- |
| B. | Colour blindness | 2. | Autosomal
chromosome 7 |
| C. | Phenylketonuria | 3. | Autosomal
chromosome 11 |
| D. | Cystic fibrosis | 4. | Autosomal
chromosome 4 |
| E. | Huntington's
disease | 5. | Autosomal 12
chromosome 12 |
184740
Match Column I with Column II and find the correct answer
| Column - I | | Column - II | |
| :--- | :--- | :--- | :--- |
| A. | Monoploidy | i. | $2 n-1$ |
| B. | Monosomy | ii. | $2 n+1$ |
| C. | Nullisomy | iii. | $2 n+2$ |
| D. | Trisomy | iv. | $2 n-2$ |
| E. | Tetrasomy | v. | n |
| | | vi. | 3n |
184741
Match the following
| List-I | | List-II | |
| :--- | :--- | :--- | :--- |
| (A) | Down syndrome | (I) | 45, X |
| (B) | Edward
syndrome | (II) | 47, XX, +13 |
| (C) | Klinefelter's
syndrome | (III) | 47, XX, +18 |
| (D) | Patau syndrome | (IV) | 47, XX, +21 |
| (E) | Turner's
syndrome | (V) | 47, XXY |
184736
Match the human genetic disorder with the causative abnormal chromosome
| A. | Sickle cell anaemia | 1. | Sex linked (X
chromosome) |
| :--- | :--- | :--- | :--- |
| B. | Colour blindness | 2. | Autosomal
chromosome 7 |
| C. | Phenylketonuria | 3. | Autosomal
chromosome 11 |
| D. | Cystic fibrosis | 4. | Autosomal
chromosome 4 |
| E. | Huntington's
disease | 5. | Autosomal 12
chromosome 12 |
184740
Match Column I with Column II and find the correct answer
| Column - I | | Column - II | |
| :--- | :--- | :--- | :--- |
| A. | Monoploidy | i. | $2 n-1$ |
| B. | Monosomy | ii. | $2 n+1$ |
| C. | Nullisomy | iii. | $2 n+2$ |
| D. | Trisomy | iv. | $2 n-2$ |
| E. | Tetrasomy | v. | n |
| | | vi. | 3n |
184741
Match the following
| List-I | | List-II | |
| :--- | :--- | :--- | :--- |
| (A) | Down syndrome | (I) | 45, X |
| (B) | Edward
syndrome | (II) | 47, XX, +13 |
| (C) | Klinefelter's
syndrome | (III) | 47, XX, +18 |
| (D) | Patau syndrome | (IV) | 47, XX, +21 |
| (E) | Turner's
syndrome | (V) | 47, XXY |
184736
Match the human genetic disorder with the causative abnormal chromosome
| A. | Sickle cell anaemia | 1. | Sex linked (X
chromosome) |
| :--- | :--- | :--- | :--- |
| B. | Colour blindness | 2. | Autosomal
chromosome 7 |
| C. | Phenylketonuria | 3. | Autosomal
chromosome 11 |
| D. | Cystic fibrosis | 4. | Autosomal
chromosome 4 |
| E. | Huntington's
disease | 5. | Autosomal 12
chromosome 12 |
184740
Match Column I with Column II and find the correct answer
| Column - I | | Column - II | |
| :--- | :--- | :--- | :--- |
| A. | Monoploidy | i. | $2 n-1$ |
| B. | Monosomy | ii. | $2 n+1$ |
| C. | Nullisomy | iii. | $2 n+2$ |
| D. | Trisomy | iv. | $2 n-2$ |
| E. | Tetrasomy | v. | n |
| | | vi. | 3n |
184741
Match the following
| List-I | | List-II | |
| :--- | :--- | :--- | :--- |
| (A) | Down syndrome | (I) | 45, X |
| (B) | Edward
syndrome | (II) | 47, XX, +13 |
| (C) | Klinefelter's
syndrome | (III) | 47, XX, +18 |
| (D) | Patau syndrome | (IV) | 47, XX, +21 |
| (E) | Turner's
syndrome | (V) | 47, XXY |
184736
Match the human genetic disorder with the causative abnormal chromosome
| A. | Sickle cell anaemia | 1. | Sex linked (X
chromosome) |
| :--- | :--- | :--- | :--- |
| B. | Colour blindness | 2. | Autosomal
chromosome 7 |
| C. | Phenylketonuria | 3. | Autosomal
chromosome 11 |
| D. | Cystic fibrosis | 4. | Autosomal
chromosome 4 |
| E. | Huntington's
disease | 5. | Autosomal 12
chromosome 12 |
184740
Match Column I with Column II and find the correct answer
| Column - I | | Column - II | |
| :--- | :--- | :--- | :--- |
| A. | Monoploidy | i. | $2 n-1$ |
| B. | Monosomy | ii. | $2 n+1$ |
| C. | Nullisomy | iii. | $2 n+2$ |
| D. | Trisomy | iv. | $2 n-2$ |
| E. | Tetrasomy | v. | n |
| | | vi. | 3n |
184741
Match the following
| List-I | | List-II | |
| :--- | :--- | :--- | :--- |
| (A) | Down syndrome | (I) | 45, X |
| (B) | Edward
syndrome | (II) | 47, XX, +13 |
| (C) | Klinefelter's
syndrome | (III) | 47, XX, +18 |
| (D) | Patau syndrome | (IV) | 47, XX, +21 |
| (E) | Turner's
syndrome | (V) | 47, XXY |