Chromosomal analysis of this karyotype reveals the mutation is a result of O A. a missing X chromosome. O B. an extra chromosome on chromosome 9. OC a deletion of a section of chromosome 21. O D. a missing Y chromosome.

Human Anatomy & Physiology (11th Edition)
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Author:Elaine N. Marieb, Katja N. Hoehn
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Chapter1: The Human Body: An Orientation
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Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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delian Genetics / 7 of 15
The karyotype diagram below represents a human female with the genetic disorder known as Turner syndrome.
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Chromosomal analysis of this karyotype reveals the mutation is a result of
O A. a missing X chromosome.
O B an extra chromosome on chromosome 9.
LO C adeletion of a section of chromosome 21.
O D. a missing Y chromosome.
phil.cdc.gov image 15006
Transcribed Image Text:delian Genetics / 7 of 15 The karyotype diagram below represents a human female with the genetic disorder known as Turner syndrome. 5 10 11 12 13 14 15 16 17 18 20 21 22 19 Chromosomal analysis of this karyotype reveals the mutation is a result of O A. a missing X chromosome. O B an extra chromosome on chromosome 9. LO C adeletion of a section of chromosome 21. O D. a missing Y chromosome. phil.cdc.gov image 15006
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