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Sam was found to be heterozygous for sickle-cell (Ss) trait. The alleles represented by the letters S and s are
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- Hemophilia is an X-linked disease associated with the inability to produce specific proteins in the blood-clotting pathway. Shown above is a family pedigree tree in which family members afflicted with the disease are shown with filled-in squares (male) or circles (females). A couple is trying to determine the likelihood of passing on the disease to their future children (represented by the ? symbol above) because the hemophilia runs in the woman’s family 4.Assuming that the woman in the couple is a carrier, what is the probability that the couple’s first son will have hemophilia?In a well-publicized paternity case, the following facts were determined: the mother, a beautiful, twice-convicted axe murderer, is blood type A. Her child, Lizzie, is type O and the alleged father, a mild-mannered felon convicted of check fraud, is type B. On the last day of the trial, another father – a missionary worker with blood type O is identified. Which of the two could be Lizzie’s father? Use the space below to support your conclusion. I am really confused with the queshtion and need help finding the answer and how to prove can somone explain the answer and show it in a punnet sqaure pleaseA couple who are a carrier of sickle-cell disease with blood type A for the female and type B for the male (assume heterozygosity for blood types). What is the probability that they will have a son with blood type B and is sickle- cell? Please show the solution.
- A man with Type AB blood is married to a woman with Type O blood. They have 2 natural children and one adopted child. Their blood types are shown below: Jane-A Bobby - B Gracie O Which child is adopted? Complete the Punnett Square below and answer the questions that follow. List the possible genotypes: List the possible phenotypes Who is the adopted child? Explain your answer using the information from the Punnett square.Duchenne’s muscular dystrophy (DMD) is an X-linked disease that causes progressive muscle weakness and is often fatal. “XD” represents the wild type allele, and “Xd,” the mutant allele. Jonah is XDXd Y and his brother Pete is Xd Y. Jonah and Pete BOTH have DMD of equal severity and phenotypes. You might have thought Jonah’s DMD would be less severe given his genotype. To better understand the situation, you investigate Jonah’s Xist chromosome region in his defective muscle cells. Which of the following is consistent with his phenotype? (Select all that apply.) The Xd-containing chromosome is inactive in defective muscle cells. The XD-containing chromosome has a methylated Xist promoter. The XD-containing chromosome has an unmethylated Xist promoter. The Xd-containing chromosome is active in defective muscle cells.Jackie is blood type O, her mother is blood type A, and she believes her father is blood type AB. Is she correct? Explain
- Luanne (AA-) and Hank (AB+) Phillips had twins, a boy and a girl. Maya (AO-) and Sam (AO-) Smith had a boy. When Luanne received her son’s birth certificate, his blood type was labeled O-. Based on the information provided, what is the best possible explanation for the O- blood type on the birth certificate Luanne received? What is the best explanation for the Smith’s son whose blood was labeled AB-?The following is a summary of the possible sickle-cell genotypes and phenotypes: AA - cojmpletely normal AS - sickle-cell trait (this person has a combination of normal hemoglobin and the abnormal, sickled form of hemoglobin) SS - sickle-cell anemia (all abnormal hemoglobin) If both parents and heterozygous for sickle-cell disease, what are the possible genotypes and phenotypes for their children?If the mother is blood type AB , the father is Blood type O . Could the daughter who has type O be their child?
- The identity of Kim's biological father is unknown, but it is thought to be either Kevin or Thomas. To determine which of the two men it is, blood typing of all the persons involved was performed. Here are the results of the blood tests, including the phenotypes and possible genotypes of each person: Rachel (mother) Type AB; genotype IA, IB Kim (child) Type A; genotype is either IA, IA (if homozygous) or IA, i (if heterozygous) Kevin (alleged father #1) Type A; genotype is either IA,IA if homozygous or IA, i if heterozygous Thomas (alleged father #2) Type O; genotype is ii There are 2 DNA bands in the "fingerprint" of each person tested: mother, child, alleged father 1, and alleged father 2. Why are there two bands for each person and not three?Sickle cell anemia is a human genetic disorder caused by an autosomal recessive allele. A couple plan to marry and want to know the probability that they will have an affected child. With your knowledge of Mendelian inheritance, what can you tell them if (1) each has one affected parent and a parent with no family history of SCA or (2) the man is affected by the disorder but the woman has no family history of SCA?Hemophilia is a sex-linked recessive trait. A male hemophiliac and phenotypically normal female have a son with hemophilia. They would like to have one more child. What is the probability of having a child without hemophilia? Explain using a Punnett square. Is it possible for a girl to be born with hemophilia? Explain.