Answer: The possible genotype for their child is Hh. All the children will be heterozygous for Huntington (Hh).
The possible phenotype for their child is Huntington disease.
Explanation: If H represents the trait for Huntington and h represents normal trait; and if Huntington trait (H) is dominant over normal trait (h), therefore the genotype of the mother who is homozygous for Huntington disease is HH and the genotype of the man who is homozygous normal is hh.
A cross between the man and woman will produce offsprings who are all heterozygous for Huntington disease Hh. Phenotypically, the offsprings will manifest as Huntington disease.
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Explanation:
blood cells are BICONCAVE DISK in shaped because they lack nucleus
Answer:
C. able to relieve hemophilia symptoms.
Explanation:
Hemophilia is a genetic disorder. It is an X-chromosome linked recessive disorder. It is caused by deficiency of functional blood clotting factor VIII. The Functional factor VIII al deficiency may be inherited or arise from spontaneous mutation.
The symptoms of hemophilia can be reduced partially by functional Factor VIII. This will help to counter functional deficiencies in factor VIII in the haemophilic individuals.
Food availability
<span>Predator populations </span>
<span>Disease and parasites</span>