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:
DNA stores that info
Explanation:
In eukaryotic cells (ex. plants and animals) the DNA is found in the nucleus of the cell. Structures called ribosomes build proteins (this process is called translation).
Answer:
A surface wave is a wave that moves along the interface of two different materials, like air and water.
Explanation:
Explanation:
The out come that mendel's observed from dihybrid crosses confirmed that each trait could be described by a pair of factors that segregated to form progeny (his first law) and further suggested that factors for multiple traits segregated independently, thus forming the basis for mendel's second law of inheritance
Hope this will help you analyse your answer
The right answser is Chromosomes.
After DNA replication during cell cycle interphase, the chromosomes are composed of two identical chromatids attached at the centromere. Each chromatide is formed of a molecule of DNA (the nucleofilament) associated with proteins, the histones, around which it winds to form nucleosomes. At the ends of each chromatid are telomeres, consisting of repetitive DNA sequences that provide protection for chromosomal endings. Telomeres and centromere do not encode genetic information, it is non-coding DNA.
