Answer:
Option D.
Explanation:
Both genes are linked to X chromosome. They are recessive diseases and a heterozygous gene, which means that two different forms of a particular gene are inherited, one from each parent.
CB : Color blindness carrier, healthy
H: Hemophilia carrier, healthy
h: Disease
cb: Disease
Mom: X(CB/H) X(cb/h) (carrier)
Dad: X(cb/H) Y (color blind man, and dominant for hemophilia - healthy)
Let's make a table
MOM/DAD | X(CB/H) X(cb/h) |
X(cb/H)Y | X(cb/H) X(CB/H) | Healthy girl for H, carrier for cb
X(cb/H)Y | X(cb/H) X(cb/h) | Healthy girl for H, sick for cb
X(cb/H)Y | Y X(cb/h) | Boy sick for cb and h
X(cb/H)Y | Y X(CB/H) | Boy healthy for CB and H
1 probable case, over 4 possible cases