Respuesta :
theres a character minimum smh but i think its d pls check though g00gle is fr33
Answer:
The correct answer is D
Explanation:
The gen for hemophilia is located in the X chromosome, making the disease a sex-linked trait.
- A woman has 2 X chromosomes, so she can carry two copies of the H/h gene. If she carries the dominant allele H in one or two copies she will have normal blood clotting. If the woman has two recessive hh alleles, she will have hemophilia.
- A man only has one X chromosome (the other sex chromosme is a Y). If that chromosome has the H allele, he will not have the disease; if he has the h allele, he will be hemophilic.
The cross is between a heterozygous woman with a normal man:
[tex]X^H X^h[/tex] x [tex]X^H Y[/tex]
- The woman produces two types of gametes: [tex]X^H[/tex] and [tex]X^h[/tex]
- The man produces two types of gametes: [tex]X^H[/tex] and [tex]Y[/tex]
As a result of a Punnett Square, the expected offspring will be:
1) [tex]X^H X^H[/tex] : normal female
2) [tex]X^H X^h[/tex] : normal female, carrier of hemophilia
3) [tex]X^H Y[/tex] : normal male
4) [tex]X^h Y[/tex] : hemophilic male
The correct answer is D: one female normal, one male normal, one female carrier, one male with hemophilia