Answer:
<h2>I think, you answer is. </h2>
<h2><u>somatosensory</u><u> </u><u>cortex</u><u>.</u><u> </u></h2>
Explanation:
<h2>Hope it helps you.....</h2>
<h3>Thank <em>you</em><em /><em>.</em><em>.</em></h3>
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Hello!
✧･ﾟ: *✧･ﾟ:* *:･ﾟ✧*:･ﾟ✧
❖ A patient is suffering from liver failure and their liver is not producing enough plasma proteins. This will result in decreased colloid osmotic pressure.
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Answer:
Pretty sure Its, (H. 0.6)
Hemophilia is carried on the X chromosome. If it is passed on to a son it came from its mother. If a daughter inherits it it could have came from either parents or even both. If from the father he himself would have been a hemophiliac. Hope this helps.
Answer:
A mutation that changes the first letter to 'C' is called<u> Frameshift mutation.</u>
Explanation:
- <u> FRAMESHIFT MUTATION </u> -: A frameshift mutation is a genetic mutation of a number of nucleotides caused by indels (insertions or deletions) in a DNA sequence that is not divisible by three. A frameshift mutation (also called a framing error or a reading frame shift) The addition or deletion may alter the reading frame (the grouping of codons) due to the triplet nature of gene expression by codons resulting in a completely different translation from the root. A frameshift mutation, instead of being added or removed, is not the same as a single-nucleotide polymorphism in which a nucleotide is substituted. In general, a frameshift mutation will cause the reading of the codons to code for various amino acids after the mutation. The first stop codon ("UAA", "UGA" or "UAG") encountered in the series would also change the frameshift mutation. The polypeptide that is formed will be abnormally short or abnormally long, and most likely will not be functional.
- Hence, the answer is<u> Frameshift Mutation</u>.
