If a female having gene for haemophilia and colour-blindness on its one X-chromosome marries a normal male then what are the chances in their offsprings :

A woman with two genes one for haemophilia and one for colour blindness on one of its X-chromosomes marries a normal man .The progeny will be

A woman with two genes one for haemophilia and one for colour blindness on one of its X-chromosomes marries a normal man .The progeny will be

A woman with two genes for haemophilic and a gene for colour blindness on one of the X-chromosome marries a normal man.How will the progeny be ?

A woman with two gases (one on each X-chromosome) for haemophilia and one gene for colour blindness on the X-chromosomes marries a normal man. How will the progeny be?

A woman with two gases (one on each X-chromosome) for haemophilia and one gene for colour blindness on the X-chromosomes marries a normal man. How will the progeny be?

The gene for haemophilia is located on the chromosome of humans.It is normally imposssible for a

A colourblind woman marries a normal visioned male. In the offspring