Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- Hemophilia is a blood disorder which is sex-linked. A woman carrier has children with a normal man. Determine the chances for girls and boys with hemophilia. [Remember that females have the XX genotype and males have the XY genotype. Do not place an allele on the Y chromosome. Example: XN Xn for female; Xn Y for male]arrow_forwardFor the following genotypes state the ABO blood phenotype. IAIA - IBIO - IOIO - IAIB –arrow_forwardTwo parents with blood types AB and B have a child who has A blood type. What is the chance that their next child will be blood type O? a 0 b 1/2 c 1/4 d 1 e 3/4arrow_forward
- If a man with type O blood has a child with a woman who has type AB blood, what are the possible blood types for the child?arrow_forwardIf two people with sickle cell traits (AS genotype) have children, what are the chances that these parents will have three children with the AS genotype. AA genoype if normal, AS is heterozygous, and SS is homozygous for sickle cell disease.arrow_forwardA mother with blood type A has a child with blood type AB. Give all possible blood types for the father of this child. Group of answer choices O B, AB A, AB A, B, O A, B, AB, Oarrow_forward
- Jan and Michael are both carriers for the cystic fibrosis allele. If Jan and Michael have five children, what the probability that three or more of the children will have the disease?arrow_forwarda couple has two children. one has o blood and other has type B.what are the most likely genotype of the parents?arrow_forwardFour children have the following blood types: A, B, AB, and O. Could these children have the same two biological parents?arrow_forward
- The alleles for Blood type O can be represented by: "00". (Two capital Os) Which of the following is the correct way to describe this genotype? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. Homozygous dominant a b Homozygous recessive Heterozygous dominant d Heterozygous recessivearrow_forwardIs this correctarrow_forwardIn a parental cross for an autosomal MOI, the ratio (Disease phenotype):(WT phenotype) differ for the scenarios: (i) the father is affected and mother is unaffected; and (ii) the mother is affected and the father is unaffected. a) true b) falsearrow_forward
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