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:
Softer? I hope this helps :)
Explanation:
Because the soil didn't have the same nutrients it has now due to lack of decomposition of other plants and animals.
The cell is in METAPHASE PHASE OF MEIOSIS. At this phase, the pairs of homologous chromosomes moves to the cell equator. These pairs of homologous chromosomes will be separated in anaphase I. The number of chromosomes remains constant until the first cell division is completed, then the chromosomes will be divided into two daughter cells.
Because they are made mostly or partly out of gas.