A couple gives birth to a healthy baby girl. As the girl grows and develops, they later find out she has Turner's Syndrome. Instead of having the genotype XX (the normal genotype for females) she is missing an X chromosome. This is determined based on the symptoms of developing no secondary sexual characteristics, and a karyotype confirming the missing X chromosomes. The family is trying to understand the cause. Which of the following choices below provides the best explanation for how the girl got Turner's Syndrome? *
A couple gives birth to a healthy baby girl. As the girl grows and develops, they later find out she has Turner's Syndrome. Instead of having the genotype XX (the normal genotype for females) she is missing an X chromosome. This is determined based on the symptoms of developing no secondary sexual characteristics, and a karyotype confirming the missing X chromosomes. The family is trying to understand the cause. Which of the following choices below provides the best explanation for how the girl got Turner's Syndrome? *
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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A couple gives birth to a healthy baby girl. As the girl grows and develops, they
later find out she has Turner's Syndrome. Instead of having the genotype XX (the
normal genotype for females) she is missing an X chromosome. This is
determined based on the symptoms of developing no secondary sexual
characteristics, and a karyotype confirming the missing X chromosomes. The
family is trying to understand the cause. Which of the following choices below
provides the best explanation for how the girl got Turner's Syndrome? *
14

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b Answered: Which phras X
Q Fichas de aprendizaje C
A docs.google.com/forms/d/e/1FAlpQLSdv6s9c6ISZpFULpxeSkekPHNA3ptICMhWÜM4XLEpCG-SGCH9/formResponse
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The mother was exposed to a mutagen during early pregnancy that altered the
genotype of her daughter.
During crossing over, the X chromosome was shuffled and traits were lost during the
process
The mother and father both carried a recessive allele which were then passed to the
daughter.
During meiosis, nondisjunction occurred and the sex chromosomes did not separate
evenly into gametes of one parent.
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