Based on the information provided by the Angus pedigree below, Princess Alta of Wey (R) is inbred. T Bonanza of Wye A Blythe of Wye Ayer of Wye B Hannah Jini of Wye P C D Bernie Dina Francis of Wye of Wye of Wye True False F Fortrel of Wye Ballista of Wye \R Princess Alta of Wye V Puck of Juryman of Wickwice Wickwire H Princetta Joy of Wye Phyllis of Wye
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- On the left side of this figure, explain why the offspringdoes not have Prader-Willi syndrome but does have Angelman syndromeThe pedigree for Queen Victoria of England, acarrier of hemophilia A, shows the transmission tosome of her descendants, including members ofmany royal families in Europe, such as Russia andSpain, but not Germany. Hemophilia A does notaffect anyone in the present British royal family.Can you explain why hemophilia A hasdisappeared from one family and appeared inothers?Marfan syndrome is a rare inherited human disorder characterizedby unusually long limbs and digits plus defects in the heart (especially the aorta) and the eyes, among other symptoms. Following isa pedigree for this disorder. Affected individuals are shown withfilled (black) symbols. What type of inheritance pattern do youthink is the most likely?
- The following pedigree shows the inheritance of a rare genetic disorder. Determine the most likely mode of inheritance, and for exam practice (unmarked on the assignment) write a clear justification for your conclusion. Remember that some pedigrees don't provide sufficient data/information to discriminate between possibilities. If that is the case, select all the possible answers. I III Tb 2 3 1 1 3 autosomal dominant autosomal recessive Osex-linked dominant Osex-linked recessive O 2 HFrank and Susan both have freckles but they're firstborn son Lawrence does not demonstrate the characteristics. What are the most likely genotype of Frank Susan and Lawrence?A young couple went to see a genetic counselor because each had a sibling with cystic fibrosis. (Cysticfibrosis is a recessive disease, and neither member ofthe couple nor any of their four parents is affected.)a. What is the probability that the female of thiscouple is a carrier?b. What are the chances that their child will havecystic fibrosis?c. What is the probability that their child will be acarrier of the cystic fibrosis disease allele?
- Cystic fibrosis is determined by simple dominant-recessive inheritance, where the trait for cystic fibrosis is recessive. Given Rnormal, r is CF gene, complete the following Punnett squareGilbert's genetic makeup is homozygous for dark hair. Jan's is homozygous for blond hair. What proportion of their children are likely to be dark-haired? Explain.A recently married man and woman discover that eachhad an uncle with alkaptonuria (black urine disease), arare disease caused by an autosomal recessive allele of asingle gene. They are about to have their first baby. Whatis the probability that their child will have alkaptonuria?
- Sam was found to be heterozygous for sickle-cell (Ss) trait. The alleles represented by the letters S and s areVictoria’s youngest child, Beatrice, gave birth to one daughter, one normal son, and two hemophilic sons. **Based on the pedigree, Alfonso XIII of Spain is phenotypically normal. Does that mean he received the normal gene from Beatrice? Why or Why not?**A man with type AB blood is married to a woman with type O blood. They have two natural childrenand one adopted child. Jane has type A blood, Bobby has type B blood, and Grace has type O blood.Which child was adopted?