Answer:
the mutation in OCA2, which is probably the oldest mutation causing albinism.
Explanation:
I think this is what you're asking for but i don't know. I'm sorry if it's not.
<span>A woman's ovary is sixteen times the size of a single sperm. This allows said sperm, or any of its friends, to penetrate the ovary with ease and precision. The ovary will also serve as the home for this sperm during its growth, proving that its larger size has multiple purposes in assisting in sperm growth.</span>
electrical energy
Explanation:
In physics, electromagnetic radiation (EMR) consists of waves of the electromagnetic (EM) field, propagating through space, carrying electromagnetic radiant energy. It includes radio waves, microwaves, infrared, (visible) light, ultraviolet, X-rays, and gamma rays.
Answer:
The reason why only 3 out of the 22 possible autosomal trisomies are seen in newborns, is because the rest of them are chromosomal abnormalities not compatible with life and thus an spontaneous abortion occurs. The embryos suffering from these trisomies do not survive for more than a few weeks in the uterus, so the miscarriage often goes unnoticed for the mother as she may not have realized she was pregnant.
The only trisomies that are allow fetuses to be born are: Patau Syndrome (trisomy 13), Edwards Syndrome (trisomy 18), and Down Syndrome (trisomy 21). Out of these three, people with Down Syndrome have the largest life expectancy.
Answer:
these statements are true
B) Insertions or deletions of single base-pairs within a protein coding sequence probably change the amino acid sequence
D) Missense mutations always change the amino acid sequence encoded by a gene
E) Nucleotide substitutions outside of the coding sequence can affect the expression of a gene.
Explanation:
B) insertion or deletion of nucleotide in coding region of DNA can change the amino acid sequence encoded.
D) missense mutation means that the change in nucleotide sequence resulting in change in amino acid sequence encoded by gene.
E) A mutation may alter the promoter of a gene, thereby affecting the rate of transcription.
