Haemophilia is an X-linked recessive disorder. A female carrier (with one normal X chromosome and one X chromosome carrying the defective gene) has a 50% chance of transmitting the defective X chromosome to her sons. Since sons inherit the Y chromosome from their fathers, they can only inherit the X chromosome from their mother. Therefore, a female carrier can pass on the disease to her sons.
The correct answer is (A) : Female carrier for haemophilia may transmit the disease to sons.
The correct answer is: (A) Female carrier for haemophilia may transmit the disease to sons.
Haemophilia is a genetic disorder that impairs the blood's ability to clot properly. It is an X-linked recessive disease, which means the defective gene causing the disorder is located on the X chromosome. Since males have only one X chromosome (XY), a single defective allele on the X chromosome will result in haemophilia. In contrast, females have two X chromosomes (XX), so a single defective allele typically does not cause the disease in females unless both X chromosomes carry the mutation.
A female who carries the haemophilia gene (heterozygous carrier) may pass on the X chromosome with the defective gene to her children. If she passes this X chromosome with the mutation to a son (who inherits only one X chromosome from his mother), the son will have haemophilia. Therefore, a female carrier of haemophilia has a 50% chance of transmitting the disease-causing allele to her sons.
Thus, the correct statement is that a female carrier for haemophilia may transmit the disease to her sons, as stated in option (A).
| Column I | Column II | ||
|---|---|---|---|
| 1. | Calotropis | p. | Invertebrates |
| 2. | Pisaster | q. | Distasteful |
| 3. | Monarch butterfly | r. | Cryptically colored |
| 4. | Frogs | s. | Cardioglycoside |
Match Column I and Column I
| Column I | Column II | ||
|---|---|---|---|
| 1 | Narrowly utilitarian argument | p | Conserving biodiversity for major ecosystem services |
| 2 | Broadly utilitarian argument | q | Every species has an intrinsic value and moral duty to pass our biological legacy in good order to future generation. |
| 3 | Ethical argument | r | Receiving benefits like food, medicine & industrial products. |
| 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 |
Find the incorrect statement among the following: n(A) In sex-linked recessive traits, the gene is transmitted from an unaffected carrier female to some of the male progeny. n(B) Accumulation of phenylpyruvic acid in the brain results in mental retardation. n(C) Individuals affected by Down’s Syndrome will have congenital heart defects and are more intelligent. n(D) Turner’s Syndrome is caused due to the absence of one X chromosome.

Match the column I with column II.
Column-I: (A) Autosomal trisomy, (B) Allosomal trisomy, (C) Allosomal Monosomy, (D) Cystic fibrosis
Column-II: (i) Turner's Syndrome, (ii) Mendelian disorder, (iii) Klinefelter's Syndrome, (iv) Down's Syndrome