A woman is heterozygous for a rare dominant autosomal genetic disease, Neurofibromatosis. She marries a normal man (homozygous recessive for Neurofibromatosis), who has Red-Green Color blindness, an X-linked recessive trait. They have children. What is the chance they will have a girl with Neurofibromatosis?
A. 25%
B. 0%
C. 50%
D. 100%