Answer:
0%
Explanation:
Achondroplasia is an autosomal dominant disorder that is expressed in both homozygous and heterozygous dominant genotypes. Since two affected parents have a normal girl child, both the parents should be heterozygous carrier for the disease. Let's assume that the dominant allele "A" is responsible for the disease. Genotype of both the parents of the girl would be "Aa". The genotype of girl with normal stature is "aa". Genotype of her normal partner is "aa".
A cross betwee aa X aa would get all the progeny with "aa" genotype. Therefore, all of their children would have normal stature and there is 0% probability for them to have a child with achondroplasia.
I think it's A not sure tho
Answer:
III3 will be "pp" lower case p
II2 will be Pp
Explanation:
As we know the trait is caused by dominant alleles. III3 is not affected so she will have two recessice alleles so 2 lower case p.
III2 is affected so the person will have one dominant allele P and one recessive. The dominant is from the father and the recessive is from the mother.
Hope that helps
Answer:
The first layers of earth are very loose, unconsolidated layers called soil, which is pretty easy to dig into, but as we go deeper we reach the bedrock, which is the hardest part of the soil profile, which is made of hard rocks and matter.This makes it harder to dig more and more deeper.
Explanation:
