Biology: The Unity and Diversity of Life (MindTap Course List)
15th Edition
ISBN: 9781337408332
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Textbook Question
Chapter 14, Problem 9SQ
Klinefelter syndrome (XXY) can most be easily diagnosed by _______.
- a. pedigree analysis.
- b. aneuploidy
- c. karyotyping
- d.
phenotypic treatment
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Joe has classic hemophilia, an X-linked recessive disease. Could Joe
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Webbed fingers is inherited as an X-linked disease An unaffected male marries an
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Chapter 14 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 14 - Prob. 1DAACh. 14 - Prob. 2DAACh. 14 - Prob. 3DAACh. 14 - Prob. 4DAACh. 14 - Prob. 5DAACh. 14 - Prob. 1SQCh. 14 - Pedigree analysis is necessary when studying human...Ch. 14 - A recognized set of symptoms that characterize a...Ch. 14 - Prob. 4SQCh. 14 - A trait that is present in a male child but not in...
Ch. 14 - Choose the statement that is incorrect. a. A son...Ch. 14 - Prob. 7SQCh. 14 - Prob. 8SQCh. 14 - Klinefelter syndrome (XXY) can most be easily...Ch. 14 - Prob. 10SQCh. 14 - Does the phenotype indicated by the red circles...Ch. 14 - G6PD deficiency is an X-Linked recessive disorder....Ch. 14 - Marian syndrome (Section 13.5) is inherited in an...Ch. 14 - Duchenne muscular dystrophy, which is inherited in...Ch. 14 - Human females have two X chromosomes (XX); males...Ch. 14 - A mutation on an autosome causes a particular...Ch. 14 - Expression of the SRY gene on the Y chromosome...Ch. 14 - The somatic cells of most individuals with Down...Ch. 14 - Mutations in the genes for clotting factor VIII...
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- Identify genetic terms and basic principles of genetics as applied to blood groups, sex-linkage, and other inherited characteristics. a. Genetics b. Inheritance theory c. Sex-linked characteristics d. Linkagearrow_forwardColor blindness is an x-linked recessive disorder. A woman who is a carrier for color blindness has children with a man who is color blind. Determine the probability that their child will be color blind. a. 0 % b. 25% c. 50% d. 100%arrow_forwardwhich is male with small testes, enlarged breasts, The genotype XXY corresponds to and decrease in body hair. a. Turner syndrome O b. Triplo-X Oc. Klinefelter syndrome d. Jacob syndromearrow_forward
- A boy is color-blind (X-linked recessive) and has a straight hairline (autosomal recessive). Which could be the genotype of his mother? Select one: А. Вbxwxw B. Bbww C. Xbxbww D. Xbywwarrow_forwardvon Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is referred to as a sex-linked disease. The recessive allele causes the disease. A man with hemophilia (xhy) marries a woman who is homozygous dominant (XHXH. A. Illustrate using a Punnett square the probability that their children will have the disease. B. Will any of their children have the disease? C. Predict the probabilities of their children having the disease.arrow_forward
- Colorblindness is a recessive x-linked trait. Which genotype represents a male with normal vision? a. XNXN b. XYN c. XnY d. XNYarrow_forwardPlease explain I don’t think this is autosomal dominant as female are more affected than male and please explain B part of the question well.arrow_forwardWhen we say that a woman is a carrier for a genetic disease or disorder it means that a. she can pass the gene only to male children b. she has 1 gene, but not the disorder c. she can pass the gene only to female children d. she has 2 genes for the disorderarrow_forward
- Many genetic disorders are inherited in a recessive manner Select one: a. False b. Truearrow_forwardBaldness is a phenomenon where individuals lose hair as they grow older. As an X-linked recessive gene, what instances do females manifest this trait? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forwardPolydactyly is a congenital physical anomaly in in humans, dogs, cats; and having supernumerary fingers or toes. If it is an autosomal dominant trait, when is a genotype of a person that shows normal phenotype? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forward
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