Answer:
C. "Because you have had one child with Tay-Sachs, you must each carry the allele. Any child you have has a 25% chance of having the disease
Explanation:
Tay-Sachs disease is an autosomal recessive disorder that means a child will acquire the phenotype or we can say disease only when both the alleles which cause disease are present in the child.
Here, in this condition neither parent has Tay-Sachs but they gave birth to a child who is suffering from the disease then it simply means that both the parents are carrier of this disease i.e. they both are heterozygous.
The cross and probability of healthy and diseased child is shown as under:
Mother Father
Parents Tt Tt
/ | | \
Off-springs TT Tt Tt tt
<u>Out of these 4 probable off-springs only 3 with genotype TT, Tt & Tt will be healthy while the 1 with genotype tt will be diseased.</u><u> </u><u>So, the probability of diseased child is 1/4 which is 25%. </u>
Also, the birth of children is an independent event so if one child has already been born with this disease then it doesn't mean that the next 3 children will be healthy for sure i.e. birth of first child cannot influence the next child. In short we can also say that in the next birth, there is still 25% chance of the child being born with this disease because previous birth has nothing to do with next birth.
The answer would be: <span>dysfunction of spermatogenesis
</span><span>Follicle-stimulating hormone(FSH) is one of the hormones that was regulated by the anterior pituitary. FSH is secreted by the gonadotropic cells and it has roles in growth and development of sexual organs. FSH will promote maturation of ovarium in female and spermatogenesis in the male.</span>
Pollution that is all around to the knowledge I’ve gathered my whole life
Answer:
characteristics
234
Explanation:
the people needs asun because the sun is shining and all tee time people needs the sun
