Answer:
The correct answer is "mutations to homologous genes".
Explanation:
The missing options of this question are:
A) morphology.
B) the pattern of embryological development.
C) biochemical pathways.
D) habitat and lifestyle choices.
E) mutations to homologous genes.
The correct answer is option E) "mutations to homologous genes".
Modern cladograms do not use physical characteristics to establish evolutionary similarities among species. Modern cladograms are constructed from evidence from molecular systematics based on similarities in mutations to homologous genes. The more similar are the homologous genes, the less different their genetic sequences are, and are considered more closely related in their evolutionary tree.
I believe they are stromal
A pedigree shows the genotypes of the family members
in autosomal recessive disorders, the diseased genes are inherited from the parents. For the person to get the disease both diseased genes should be there in the genotype as its a recessive disorder.
the dominant gene - H
recessive gene - h
for a person to get a disease, genotype should be hh, as its autosomal recessive. If the person is normal he/ she could have the genotype HH or could be Hh and thats called a carrier.
the offspring will receive one gene from the mother and one from the father
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