Colour blindness is a disease usually affecting man but the factor for it is transmitted to the children always by woman. This is because particular factor is located on
Colour blindness is a disease usually affecting man but the factor for it is transmitted to the children always by woman. This is because particular factor is located on
- A
$X$ chromosome
- B
$Y$ chromosome
- C
Both $X$ and $Y$ chromosomes
- D
Autosome
Similar Questions
Colour blindness is
Colour blindness is
$A$ : The posssibility of a female becoming a haemophilic is extremely rare.
$R$ : Mother of such a female has to be carrier and father should be haemophilic
$A$ : The posssibility of a female becoming a haemophilic is extremely rare.
$R$ : Mother of such a female has to be carrier and father should be haemophilic
One of the following is not true to haemophilia
One of the following is not true to haemophilia
Which one of the following symbols and its representation, used in human pedigree analysis is correct?
Which one of the following symbols and its representation, used in human pedigree analysis is correct?
Which is correct for inheritance of autosome linked recessive gene?
Which is correct for inheritance of autosome linked recessive gene?