Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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1) A variety of abnormalities in the numbers of sex chromosomes exist because of nondisjunction during gametogenesis. Discuss the signs and problems associated with conditions such as Klinefelter and Turner syndromes.
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- True or False: When an individual generates gametes via meiosis the gametes either receive all of their maternal alleles or all of their paternal alleles? b) Explain your answer.arrow_forwardAnalyze the karyotype shown. Indicate if it is a chromosomal male or achromosomal female. If the karyotype is normal, write the word normal under name or description. If the karyotype is abnormal, name or describethe disorder.arrow_forwardThe inheritance of Huntington Disease can be explained by the concept of haplosufficiency. Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a b True. True but only is both parents were homozygous dominant for the disorder. False. d It is impossible to tell with the information that has been provided.arrow_forward
- Demonstrate how males are at an increased risk of sex-linked recessive traits by crossing a female who is a carrier for Hunter syndrome with a normal male. The genotypes involved are XH, Xh, and Y. State the genotypes and phenotypes of the offspring.arrow_forwardDetermine the probability of the following outcome if two individuals heterozygous for the a specific disease were to produce offspring with the assigned phenotype. (6 offspring, 5 normal and 1 with disease.) Father and Mother are both heterozygous for the diseasearrow_forwardExplain the genetic alterations resulting in chromosomal aberrations and their relationship to disease processes such as trisomy 21 and Philadelphia-chromosome linked chronic myelocytic leukemia.arrow_forward
- briefly describe how chromosomal disorders happen, explaining non disjunctionarrow_forwardNondisjunction which can affect sex chromosomes as well as autosomal chromosomes as a common cause of genetic disorders. Use the space provided to illustrate the process of nondisjunction with the end result being that one cell exhibits in the monopsony me while other one exhibits trisomy. Hint: a sperm will fertilize the egg and add it’s chromosome in the last step)arrow_forwardDiscuss and compare the source (mechanism) and types of increased mutations in older mother oocytes versus older father sperm (ch 4 and ch 7.) (Diagrams may be helpful if needed to convey your thoughtsarrow_forward
- X( 13 19 Karyotype 5 2 ( ( }{ } } } } 14 20 16 }} 17 18 Chromosomal Aberrancy/Name of Syndrome: Description of Symptoms:arrow_forward8. Identify the following. Gene found on Y chromosome but not X chromosomes Protein coded for by SRY gene Function of testis determining factor (TDF) Organ that secretes testosterone and Mullerian inhibiting factor (MIF) Hormone that promotes development of external genitalia along male line Protein that transforms Wolffian ducts into male reproductive tract organs Organ that develops in the absence of TDF SRY gene sex-determining region Y protein initiating male sex determination Testosteronearrow_forwardDiscuss the mechanisms that lead to erroneous chromosome duplication, mention how they effect the development of Down’s syndrome.arrow_forward
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