Aneuploidy is a type of chromosomal disorder where the number of chromosomes is not an exact multiple of the haploid set. This is primarily caused by the addition or deletion of chromosomes rather than changes involving substitution, translocation, or inversion of chromosome sections. Let us explore why options (b) and (c) are the correct answer for this question.
In conclusion, aneuploidy is directly related to changes in chromosome number through addition and deletion, not through rearrangement or substitution of chromosome parts.
| List - I Type of Inheritance | List – II Example | ||
| A. | Incomplete dominance | i. | Blood groups in human |
| B. | Co-dominance | ii. | Flower colour in Antirrhinum |
| C. | Pleiotropy | iii. | Skin colour in human |
| D. | Polygenic inheritance | iv. | Phenylketonuria |
| List-I | List-II |
| A. Histones | III. Positively charged basic proteins |
| B. Nucleosome | IV. DNA wrapped around histone octamer |
| C. Euchromatin | I. Loosely packed chromatin |
| D. Heterochromatin | II. Densely packed Chromatin |
| List-I | List-II |
| A. Metacentric chromosome | I. Chromosome has a terminal centromere |
| B. Sub-metacentric chromosome | II. Middle centromere forming two equal arms of chromosome |
| C. Acrocentric chromosome | III. Centromere is slightly away from the middle of chromosome resulting into two unequal arms |
| D. Telocentric chromosome | IV. Centromere is situated close to its end forming one extremely short and one very long arm |