Answer:
The correct answers are "heterozygous", and "homozygous dominant".
Explanation:
Galactosemia is a condition where people are not able to process the sugar galactose. People with this condition have one gene mutated, which does not allow the proper synthesis of the enzyme that breaks down galactose. Galactosemia is inherited as an autosomal recessive genetic condition, therefore, only children that are homozygous recessive develop the condition. Children that are heterozygous or homozygous dominant, will not develop galactosemia.
Answer:
Almost all of the cells in your body share the same DNA as was found in that first cell. Eyes and heart are so different because different set of problems are made in the various eyes and heart cell
Explanation:
a
This is possible because of the length of the protein. It is always possible to add more amino acids and synthesize new protein and every new addition increases the number of possibilities drastically.
Answer: Base pairs are formed when adenine forms a hydrogen bond with thymine, or cytosine forms a hydrogen bond with guanine. The second part of a nucleotide is the phosphate, which differentiates the nucleotide molecule from a nucleoside molecule.
Explanation:
The answer would be, if I understand correctly, skeletal and smooth muscle tissue both help the body move, and give the body form. The skeletal structure give the body structure, and the muscles help the body move.
