The gene for haemophilia is located on the $X$ chromosome. Hence,it is normally impossible for a:

  • A
    haemophilic father to pass the gene to his daughter
  • B
    carrier mother to pass the gene to her daughter
  • C
    carrier mother to pass the gene to her son
  • D
    haemophilic father to pass the gene to his son

Explore More

Similar Questions

Examples of congenital diseases are

Persons who are colourblind cannot distinguish between which of the following colours?

With the help of the given pedigree,find out the probability for the birth of a child having no disease and being a carrier (has the disease mutation in one allele of the gene) in the $F_3$ generation.

Provide detailed information about Sickle-cell anemia and Phenylketonuria $(PKU)$.

$A$ normal woman whose father was colourblind marries a normal man. What kinds of children would be expected and in what proportion?

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo