.1. A child is born with a rare genetic disease, Heterotaxy Visceral, HTX1.a. Determine what are/is the possible combinations of phenotypes and genotypes the parents of this child will have. A biologically sound logical answer is required here. (1 mark)b. Describe the condition (in 3 sentences or less). (0.5 mark)c. Identify the condition in terms of a gene map locus. (0.5 mark)2. Given a mating between a male with blood type(s) B and Rh- and a female with blood type(s) O and Rh+Respond to the following queries:a. What are (all) the probable genotypes and phenotypes of the offspring of thismating? (2 marks).b. What role do glycoproteins and glycolipids play in blood group specificity?
Q.1 aHeterotaxy visceral, HTX1 is an X-linked disease that results in the randomarrangement of internal organs which cause abnormalities in the chest and abdomen.The organs affected include the…
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