Answer:
Metaphase ⇒ Chromosomes line up in the middle of the cell
Prophase ⇒ DNA condenses to form chromosomes
Anaphase ⇒ Each chromosome separates and moves to opposite ends of the cell
Telophase ⇒ Nuclear membranes form around each set of chromosomes
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.
C. Specialized cells may lose the ability to reproduce.
Answer:
C. They are made from many carbon atoms
Explanation: