Answer:
An autosomal dominant gene is one that occurs on an autosomal (non-sex determining) chromosome. As it is dominant, the phenotype it gives will be expressed even if the gene is heterozygous.
The chances of an autosomal dominant disorder being inherited are 50% if one parent is heterozygous (NL) for the mutant gene and the other is homozygous for the normal (NN), or 'wild-type', gene. This is because the offspring will always inherit a normal gene from the parent carrying the wild-type genes, and will have a 50% chance of inheriting the mutant gene from the other parent. If the mutant gene is inherited, the offspring will be heterozygous for the mutant gene, and will suffer from the disorder. If the parent with the disorder is homozygous for the gene, the offspring produced from mating with an unaffected parent will always have the disorder.
Explanation:
Explanation:
A-Oral Cavity
B-Mouth
C-Pharynx
D-Oesophagus
E-Lever
F-Stomach
G- Gallbladder
H- Doudenum
I- Large Intestine
J- Small intestine
K- Appendix
L- Rectum
M-Anus
The function performed in F is that,it mixes the food thoroughly with more digestive juices.
The function performed in M is that ,it allows the control of stool.
A is a correct answer.
Dermis is does not had contain significant amounts of the protein collagen.
Hope it helped you.
-Charlie
That this is the desired response at this stage of gestation
