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.
Mitosis - Asexual, diploid, 1, 2, during the synthesis phase.
Meiosis- sexual, haploid, 2, 4, during the synthesis phase.
Some causes could be the mother smoking, drinking, doing drugs etc. Or even simply her body doesn’t fully accept the baby growing inside her so it acts out against it. Sounds strange but it happens. Also if the mother is sick with Zika or another virus, it can harm the baby’s growth.
The oxygen in the water molecule attracts the most electrons and in so doing attracts a slightly negative charge.
The protein structures can be classified into four levels, namely the primary structure, secondary structure, tertiary structure, and quaternary structure. The primary structure is the simplest of all the structures. When all the hydrogen bonds are disrupted, the secondary, tertiary and the quaternary structures gets disrupted, which leads the protein to the most simplest structural form, that is the primary structure. In this structure, the a carbon atom is bonded to hydrogen atom, carboxyl group, amino group, and an 'R' group.
