Answer:
The correct answer is codominance.
Explanation:
It is given in the question that the genotype of Martin is HbS/HbS, and is exhibiting sickle cell anemia with unusual hemoglobin. On the other hand, the genotype of Cindy is HbA/HbA, which shows that she possesses normal hemoglobin. Both of them have a child, Mary who as usual is exhibiting genotype HbS/HbA.
This shows that Mary has acquired both the alleles for sickle cell anemia from her parents, and thus, is demonstrating both unusual and normal form of hemoglobin. Sickle cell is a condition that does not demonstrate the phenomenon of complete dominance, as it is a codominant trait.
A phenomenon in which the features of both the alleles are expressed in the phenotype is termed as codominance. Hence, Mary is demonstrating a codominance pattern.
Answer:
it maintains this because of more exchange points on the cell with more surface area comes more ports of entry and exit for materials rather a simple concept
Explanation:
Do you still need help with this question
Take the place of part of an mRNA within the ribosome.
Rna triplets
The nucleotide sequence copy of a gene is present in the mRNA. Each amino acid is represented by a triplet of the four nucleotide bases that make up the genetic alphabet. The relationship between triplet sequences and amino acids is known as the genetic code.
A codon is a triplet of RNA nucleotides that codes for a particular amino acid. To the ribosome, where translation takes place, the tRNA transports certain amino acids. During translation, the anticodons in the tRNA bind to the codons in the mRNA templates. It is essential for the codon and anticodon to interact in order to pair the codon with the appropriate amino acid.
In mRNA, each trio of nucleotides is referred to as a codon, and each codon designates a certain amino acid (hence, it is a triplet code).
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