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.
Answer:
genetics
Explanation:
calico cats must also inherit a gene unrelated to the X and Y chromosomes that codes for white fur. Because male cats have one X chromosome with code for black or orange and one Y chromosome with no color genes, they cannot technically be calico. About one in every 3,000 calico cats is born a male, and, unfortunately, don't live as long as female calicos due to their genetic abnormalities. XXY Syndrome renders male calicos sterile and can be the root cause of many other health problems
Answer:
WOULD HAVE HELPED IF I HAVE STUDIED THIS TOPIC I AM EXTREMELY SORRY
Explanation:
True
I think, could be wrong
Answer: B)
humans and chimps share a common ancestor.
Explanation:
