Differentiate between genotype and phenotype

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Question

1. Differentiate between genotype and phenotype and give examples of each.

2. Differentiate between autosomal dominant, autosomal recessive, and X-linked recessive inheritance modes.

3. A father is a carrier for cystic fibrosis. The mother is also a carrier. What is the occurrence risk for their offspring? Draw a Punnett square to demonstrate the inheritance.

4. A father expresses Huntington disease. The mother is healthy. What is the recurrence risk for their offspring? Draw a Punnett square to demonstrate the inheritance.

5. A mother is a carrier for hemophilia A. The father is healthy. What is the occurrence risk for their offspring? Draw a Punnett square to demonstrate the inheritance.

6. If a mating pair has two children and neither of the children is affected by autosomal dominant disease X for which the father is heterozygous, what is the likelihood of the next child inheriting the disease? Does the risk increase, decrease, or remain the same?

Reference no: EM133814873

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