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- 5.__When counseling parents about genetic transmission of an X-linked disorder, which concept does the nurse keep in mind? a. An X-linked disorder can be traced through the paternal lineage. b. A female can only pass an X-liked disorder to a son c. A male can pass an X-linked mutation to a son or a daughter d. A male with a mutation in an X-linked gene will manifest the disease.6. Hemophilia causes severe bleeding from minor wounds. The blood is unable to clot properly because one of the factors necessary for clotting is missing. Hemophilia is an inherited sex-linked recessive disorder transmitted on the X chromosome by mothers to their sons. i) A woman inherited the gene for hemophilia from her mother and marries a man who iş normal and has no hemophilia. What is the possibility that her children can have hemophilia?问题13 Achondroplasia (dwarfism) is an example of a dominantly inherited disease. Individuals who have the dominant gene (A) have the dwarfism phenotype, while normal height is recessive (a). What is the probability of having children with achondroplasia between a normal height female and a heterozygote achondroplasia male? 100% 75% 25% 50%
- 1. Is this trait autosomal recessive or autosomal dominant? 2. What is the genotype of II-3? 3. Circles that are shaded in means the individual has the condition. True or False? 6 4. The horizontal line connecting Il-4, I-5, and Il-6 means they are 5. What is the genotype of III-2? 4 6. Parents 3 and 4 in the first generation are looking to have a fourth child. What is the probability that the new baby would have the condition?6. A man with X-linked colorblindness marries a woman with no history of ibba colorblindness in her family. The daughter of this couple marries a normal man noitenmot and ended up hone daughter, and their daughter also marries a normal man. This mont blast couple has already had a child with color blindness. do sri ni novig A) What is the chance that next child will be color blind? B) What is the chance that this last couple will have an affected daughter? (d #50x²50 (State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntingtons disease, and hemophilia A.
- 1. Study the given alleles. Write the correct phenotype for each genotype. X – normal Gen otype xC - Color-blind Phenotype XX XY XXC xCY 2. Study the given alleles. Write the correct genotype for each phenotype. xH - Hemophiliac Phenotype X- normal Gen otype Hemophiliac female Hemophiliac male Normal female carrier of the gene Normal male Normal female 28 3. Determine the genotype and phenotype of the offspring. A color-blind mother (XCx) married a normal sighted (XY) father. Genotype: Phenotype: Genotype: Phenotype: Genotype: Genotype: Phenotype: Phenotype: a. There are b. There are c. There are d. There are % normal sons. % normal daughters. % color-blind sons. % color-blind daughters. % normal female, carrier of the disorder. or or or or e. There are or1. What role does a patient's genetics have in their symptoms of muscular dystrophy? What causes various mutations to cause distinct symptoms? (two to three sentences) (Think about why various mutations in different genes cause different illnesses.)2. What can family history teach you about a patient's muscular dystrophy inheritance and, hence, genetic basis? (two to three sentences)3. The X-chromosome contains the mutation that causes Duchenne Muscular Dystrophy (DMD). Explains how this impacts DMD inheritance and why DMD patients are disproportionately male. (two to three sentences)b. The following diagram shows a family tree of individuals with haemophilia. B i. Based on an X-linked recessive pattern of inheritance, work out the likely genotypes of the individuals indicated by the letters. Individual A Individual B Individual C GENOTYPE ii. If individual C has children with a normal male, what are the chances that they will have haemophilia? Explain your answer fully. iii. If individual C has children with a normal male, what are the chances that their daughters will be carriers of the condition? Explain your answer fully.
- 5. A man who is not bald married a non bald female whose mother is bald. A. What is the chance that the couple will have a bald son? B. What is the probability that the couple will have a bald daughter? What is the chance that the couple will have a nonbald daughter? C.1) having dimples D is dominant over not having dimples d. A dimples woman whose father had no dimple and whose mother did have dimples marries a man whose mother had no dimples, whose whose father had no dimples and whose grandparents on his father's side did have dimples. What is the genotype of the woman what is the genotype of the man 2) Deafness in cocker spaniels is inherited.The allele for deafness is recessive to the allele for normal hearing. Two cocker spaniels with normal hearing are mated together. They produce a little of eight puppies, two of which are found to be deaf. Give the genotype of the parent. How many of the puppies will be unable to produce deaf offspringExplain the following1. A couple comes to a genetic councilor concerned about their chances of having a baby with cystic fibrosis disease. The husband had a sibling die of the disease. What are the chances that he is a carrier?