Answer:
Hemophilia is a sex-linked recessive disorder in which a person's blood do not clots and he can bleed to death even after minor injuries because blood will keep running due to a small cut.
It is a recessive trait which means that even if one normal gene is present along with Hemophiliac gene, the person will not have the disease and he will be the carrier.
Question: What will be their children’s possible phenotypes?
If a woman who is a carrier for hemophilia marries a hemophiliac man, their genotypes can be denotes as :
Here H, indicate normal gene and small h indicate defected (hemophilia) gene.
Parents: XHXh X XhY
Offspring: XHXh : XHY: XhXh: XhY
Phenotype of offspring:
XHXh: The child will be daughter and normal (25 % chances)
XHY: The child will be son and normal (25 % chances)
XhXh: The child will be girl and Hemophiliac (25 % chances)
XhY: The child will be son and Hemophiliac (25 % chances)
Hope it helps!
Answer:
The answer is C.
Explanation:
At first, an enzymes called Helicase unwind the double helix in a DNA .
Answer:
Can I get brainiest answer Mitochondria Lysosomes vacuole
Answer:
The correct answer is - 75% or 3/4.
Explanation:
In the given question, there is a cross between III-6 and III-7 that produced two double eyes monsters and expected one more. As given in the image that the A or single eye is dominant over the a or double eye then both parents must be heterozygous as they produced double eye offspring (aa) and they do have only one eye.
then chances of single eye offspring would be -
cross: Aa and Aa
gametes: A, a and A, a
Punnett square:
A a
A AA Aa
a Aa aa
so there are 75% chances to have a single eye and 25% chances for a double eye.
The first step to DNA replication is to unzip the double matrix which also means that they will break the double matrix.
