The independent assortment of genes is a principle of Mendel and of genetics. Since humans are diploid organisms (they have 2 copies of their genetic information), we have that each gamete carries one of the two available alleles for each feature. These gametes are created in equal proportions.
We have that both parents are heterozygous for a feature, lets say H. Thus, their genotype is Hh. Hence, the child will get with probability 50%=1/2 H from the father and 50%=1/2 h from the father; same from the mother. By doing a Punnett square, we get that there is 1/4 chance that the child is HH, 1/2 chance that it is Hh and 1/4 that is hh. Since the disease is recessive (so both alleles are needed), we have that the chance that the kid has the disease is 1/4.
Answer:
it is called a ledgar
Explanation:
Dont really know how to explain but hopefully it's right
There are three types of RNA involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribisomal RNA (rRNA). All three of these nucleic acids work together to produce a protein. The mRNA takes the genetic instructions from the nucleus to the cytoplasm, where the ribosomes are located.
