2. Huntington's disease is a degenerative disease of the nervous system which does not show up until age 40. It is caused by a dominant gene. John's father just began to show the symptoms. What is the chance that John will have the disease?
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- The following pedigree shows the pattern of inheritance of red-green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in black. What is the chance that a son of the third-generation female indicated by the arrow will be color blind if the father is not color blind? If he is color blind?Cystic fibrosis is an autosomal disease that mainly affects the white population, and 1 in 20 whites are heterozygotes. Genetic testing can diagnose heterozygotes. Should a genetic screening program for cystic fibrosis be instituted? Should the federal government fund it? Should the program be voluntary or mandatory, and why?A couple who are about to get married learn from studying their family histories that, in both their families, theirunaffected grandparents had siblings with cystic fibrosis(a rare autosomal recessive disease).a. If the couple marries and has a child, what is theprobability that the child will have cystic fibrosis?b. If they have four children, what is the chance that thechildren will have the precise Mendelian ratio of 3:1 fornormal:cystic fibrosis?c. If their first child has cystic fibrosis, what is theprobability that their next three children will be normal?
- Albinism is a recessive disorder where there is a lack of melanin. Andrea and her husband Claude both have normal skin pigmentation. Andrea’s mother has the albino phenotype, but her father and her brother do not (normal pigmentation). Claude’s parents are both normal, but he has a sister who has the condition (is albino). Answer the following questions If Andrea and Claude are carriers for the albino allele, what is the probability that they have an albino child? If Andrea and Claude have a second child, what is the probability this child be normal (non-albino)? NOTE: Draw a punnet square or show your work.What are the genotypes of the mother and father in the pedigree below? The pedigree shows albinism (an autosomal recessive trait). The shaded shapes represent albino individuals. a. mother - homozygous dominant; father - homozygous dominant b. mother - heterozygous; father - homozygous recessive c. mother - homozygous recessive; father - heterozygous d. mother - heterozygous; father - heterozygous e. mother - homozygous dominant; father - homozygous recessiveBased on the observed inheritance pattern and ratio of phenotypes, what are the genotypes of the affected children? Select an answer and submit it. For keyboard navigation, use the up/down arrow keys to select an answer. a) If c- = Cystic Fibrosis, the children are c-/c-. b) If c- = Cystic Fibrosis, the children are C/C. c) If c- = Cystic Fibrosis, the children are C/c-. d) If c- = Cystic Fibrosis, the children are C.
- Using the given pedigree chart, suppose individuals III-1 and III-2 are expecting their sixth child. What is the chance (percent) that the sixth child will have the sickle cell trait? Read the following family history and draw a pedigree to determine the inheritance pattern for achondroplasia. Once the pedigree is assembled , label the genotypes of each individual using a capital "A to represent the dominant allele and a lower case "a " to represent the recessive allele and create a key to identify which version is the achondroplasia allele. If you are unsure of the genotype , label the individual with a "" in place of the unknown allele. Family History : Jada and Noel , both of short stature, have been married for twenty years. They have three children : an eighteen - year-old boy named Shawn , of short stature ; a fifteen- year- old boy named John , of short stature ; and a twelve -year -old girl named Ann , of average height Noel and Jada also had a male child bom with severe achondroplasia who died six months after birth from respiratory failure . Noel's father was of short stature , while his mother was average height . Noel has a brother and a…Answer 2 Duchenne muscular dystrophy is a sex-linked recessive disorder characterized by a progressive loss of muscle tissue. Neither Carla nor Rudy has Duchenne muscular dystrophy, but their first son does have it. What can you say about Rudy's or Carla's genotype in relation with the disorder? If the couple has a second child, what is the probability that he or she will also have the disease? Show your answers with a Punnet square.
- Use the following parents to create a Punnet Square and answer the question. Cross a heterozygous father with a homozygous recessive mother. (you can use the letter A for your parental genotypes) What percent of the offspring will be homozygous recessive?Assume that attached earlobes is an autosomal recessive trait with 47% penetrance. If one parent is heterozygous (Aa) and the other homozygous recessive (aa) for the attached earlobe gene, what is the probability that their first child will have attached earlobes? Show your calculation, with labels. a. 50%b. 11.75% c. 25%d. 23.5% e. 75%Two healthy parents have a child who is later diagnosed with cystic fibrosis. What is the genetic term for this kind of disease? Using Mendel’s pattern, pick a letter for this gene and give the genotypes of the parents and the child. What are the odds that their next child will also have cystic fibrosis?