Susan was born with the genetic disorder Cystinuria although neither of her parents has the disease. Her only sibling, an older sister, is also not affected by the disease. Which pedigree below accurately shows the inheritance of Cystinuria in Susan's family? B O Pedigree A
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- Ann's family has a history of cystic fibrosis, a recessive genetic disease. In the pedigree, family members who are afflicted with the disease are shown in red. Members who are unafflicted may or may not be carriers. Which of the given family members can be identified definitively as unafflicted carriers of cystic fibrosis? Unafflicted carriers Ann Answer Bank father aunt's husband grandmother sister uncleO Huntington's Disease is a rare neurodegenerative disorder caused by a defective gene. A pedigree is shown below with a family that is affected. Describe the pattern of inheritance that Huntington's Disease is following. Justify your answer with reference to the diagram. Use proper notation (II-3, etc.) when referring to individuals. II 2 3 6 8 II 1 2 3 4 5 7.People with polydactyly have more than five fingers or toes on their hands or feet. Polydactyly results from an autosomal dominant genetic disorder. Draw a pedigree for a family with polydactyly, using the following information: Zack has polydactyly but his wife, Zoe does not. Zack and Zoe’s daughter Yolanda has polydactyly but their son Yogi does not. Yolanda has two children with her husband, Xavier, who does not have polydactyly: Wilma, who is normal and Wade, who has polydactyly. Use your pedigree to determine what is Zoe's genotype. A) DD B)dd C)Dd
- Ⓒ Macmillan Ann's family has a history of cystic fibrosis, a recessive genetic disease. In the pedigree, family members who are afflicted with the disease are shown in red. Members who are unafflicted may or may not be carriers. Which of the given family members can be identified definitively as unafflicted carriers of cystic fibrosis? Ann (n 2 grandmother Incorrect Unafflicted carriers female cousin aunt's husband father Answer Bank uncleRefer to the pedigree below which shows inheritance for achondroplasia (dwarfism), a dominantly inherited trait (denoted as D), which are the darkened circles and squares. Dwarfism (darkened shapes) are dominantly inherited, while normal height is recessively inherited (hh). Based on the pedigree, what is the correct genotype for individual #II-6? Dominant Autosomal Pedigree 2 II 2 3 II 1 2 3 6 9 10 Dd DD DD or Dd ddBelow is a pedigree chart for a family that has a history of Alkaptonuria. Individuals infected with this condition can have darkened skin, brown urine, and can suffer from joint damage and other complications. Given this pedigree answer the following questions. Given the data in the pedigree chart is this genetic condition autosomal dominant or autosomal recessive? What are the genotypes for #1, #2, and #3? If either of the 4th generation "aa" females were to mate with a homozygous dominant male would any of their offspring illustrate the phenotype? Why or why not?
- Cystic fibrosis is a genetic disease that causes an abnormal production of mucus which in turn can cause damage and infection to the lungs and other organs. In the following pedigree, black indicates all those persons afflicted with cystic fibrosis (square symbols are males, circles are females). There's a healthy couple and they have two children. One is a 23-year-old daughter with cystic fibrosis who is married to a 24-year-old male who is healthy. The other child is a 15-year-old son who is healthy After studying the pedigree, write a logical hypothesis suggesting the cause of cystic fibrosis in terms of dominant or recessive alleles. On the basis of your hypothesis, write an appropriate genotype for both of the parents. Using a Punnett square, what is the probability of the parents having a child with cystic fibrosis? If the daughter's husband is a carrier of cystic fibrosis, what is the probability that they have a child with cystic fibrosis? Show your Punnett square.For the trait being studied, what type of inheritance pattern is shown in the pedigree?Draw a pedigree to depict the following family: One couple has a son and a daughter with normal skin pigmentation. Another couple has one son and two daughters with normal skin pigmentation. The daughter from the first couple is married to the son of the second couple and they had three children. Their son and one daughter have albinism; their other daughter has normal skin pigmentation.
- Grandma Jade is affected with tuberous sclerosis, she grows benign tumors, and the trait is under control with her doctors. She is married to Grandpa Phil, who does not have the trait. Out of their four children, only one, Michael, has tuberous sclerosis. Complete the Punnett Square and indicate their genotypes.The second pedigree involves albinism, an autosomal recessive trait. A couple has a son with normal pigmentation, a daughter with normal pigmentation, and an albino son. Another couple has three children, a son with normal pigmentation and two daughters with normal pigmentation. The daughter from the first couple marries the man from the second couple and they have three children together: an albino son, an albino daughter, and a daughter with normal pigmentation.Draw the pedigree on the next pageAnn's family has a history of cystic fibrosis, a recessive genetic disease. In the pedigree, family members who are afflicted with the disease are shown in red. Members who are unafflicted may or may not be carriers. Which of the given family members can be identified definitively as unafflicted carriers of cystic fibrosis?