Answer:
Roots
Explanation:
The cells split into two of the same copy of itself (unless a bug has occurred, in which case a malform will occur), and the two copies are known as the offspring. In this case, only one pair of genes is inherited, and will continue to be the pair that is passed down (if no malform occurs).
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Answer: The probable genotype of the patient is a homozygous recessive allele (SS)
Explanation: Sickle cell is a recessive disorder, therefore it must occur in a homozygous state in order to manifest phenotypically. When it occurs in a heterozygous state AS, the dominant allele A will overshadow its effect. Sickle cell is a genetic disease caused by abnormal haemoglobin in the blood which gives the red blood cells a sickle shape denoted as S. A normal haemoglobin gives the red blood cells a disc shape and its denoted by A.