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:
Answer:
i think its a im not sure though
Answer:
D
Explanation:
During metaphase of cell division, the chromosomes line up in the metaphase plate and the spindle fibers from the poles extend and attach to the centromeres of the chromosomes. The spindle then contracts and pull different chromosomes to the opposite poles of the cell before the parent cell divides. If spindle fibers do not form, then the chromosomes will not separate during anaphase.
Therefore, the final cell after mitosis will be a cell with double the number of chromosomes -because if you remember, during interphase, genetic material is replicated so each daughter cell can have its copy-. Due to quality control in the process of cell divisison, this cell will mostly undergo apoptosis, otherwise, it could develop into cancer.
The two lower leg bones are called the tibia and the fibula
Answer:
don't know for sure sure but i would think branching
Explanation:
I think this cause of subspecies ( Bengal, Sumatran and Siberian tigers)
