Based on the pedigree, drag a claim about the inheritance pattern of sickle cell anemia into the appropriate box. Drag an evidence statement into the appropriate box to justify the claim. Claim Evidence! :: Claim 1-Sickle cell anemia is inherited in an autosomal recessive pattern. :: Claim 2-Sickle cell anemia is inherited in an autosomal dominant pattern. Evidence 1-Individual 11 has sickle cell anemia, but her parents do not. :: Evidence 2-Individuals 8 and 9 have sickle cell anemia, and their father, individual 3, is also affected. :: Evidence 3-Individual 1 has sickle cell anemia, but his children do not.
Based on the pedigree, drag a claim about the inheritance pattern of sickle cell anemia into the appropriate box. Drag an evidence statement into the appropriate box to justify the claim. Claim Evidence! :: Claim 1-Sickle cell anemia is inherited in an autosomal recessive pattern. :: Claim 2-Sickle cell anemia is inherited in an autosomal dominant pattern. Evidence 1-Individual 11 has sickle cell anemia, but her parents do not. :: Evidence 2-Individuals 8 and 9 have sickle cell anemia, and their father, individual 3, is also affected. :: Evidence 3-Individual 1 has sickle cell anemia, but his children do not.
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
Publisher:Michael Cummings
Chapter11: Genome Alterations: Mutation And Epigenetics
Section: Chapter Questions
Problem 5QP: Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of...
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Introduction
Sickle cell anemia : in this disease the RBCs become sickle shaped, due to which the WBCs attack on them and phagocytose them resulting in decrease in blood RBC count and causes anemia.
This disease is an Autosomal recessive disease. The disease is controlled by a single pair of allele HbA and HbS, the gene HbS is defective while HbA is normal gene.
The organisms with homozygous defective form of gene i.e. HbSHbS are infected with the disease.
While those who are heterozygous for the gene will be carrier of the disease, and such parents can transfer this disease to their offspring even when they themselves are not affected.
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