A man with a pointed nose and a woman with a round nose have a daughter with a round nose. This daughter has Turner Syndrome (genotype XO: one X chromosome). Nondisjunction must have occurred in melosis 2 of the mother More than one of the answers is correct Nondisjunction must have occurred in meiosis 1 of the father Nondisjunction must have occurred in meiosis 1 of the mother Nondisjunction must have occurred in meiosis 2 of the father

A man with a pointed nose and a woman with a round nose have a daughter with a round nose. This daughter has Turner Syndrome (genotype XO: one X chromosome). Nondisjunction must have occurred in melosis 2 of the mother More than one of the answers is correct Nondisjunction must have occurred in meiosis 1 of the father Nondisjunction must have occurred in meiosis 1 of the mother Nondisjunction must have occurred in meiosis 2 of the father

Name: The gene for nose shape is found on the X chromosome. Round nose is do
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Description: The gene for nose shape is found on the X chromosome. Round nose is dominant to pointed nose.Human individuals with XXY (an additional X chromosome) are male. Individuals with XO (only one X chromosome) are female. For the following family, identify

Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter20: Chromosomes And Human Genetics

Section: Chapter Questions

Problem 2CT: Human sex chromosomes are XX for females and XY for males. a. With respect to an X-linked gene, how...

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Assume that color blindness is a recessive character on the X chromosome. A man and woman with normal vision have the following offspring: a daughter with normal vision who has one color-blind son and one normal son; a daughter with normal vision who has six normal sons; and a color-blind son who has a daughter with normal vision. What are the probable genotypes of all individuals?
In humans, XO individuals are females with Turner syndrome and XXY individuals are males with Klinefelter syndrome. Red-green color blindness is caused by an X-linked recessive allele. Suppose a color-blind man and a woman with normal vision and no family history of color blindness had a daughter who was color blind and had Turner syndrome. Which event could have given rise to this offspring? Nondisjunction at meiosis I in the mother Nondisjunction at meiosis II in the mother Nondisjunction at meiosis I in the father Nondisjunction at meiosis II in the father Nondisjunction at either meiosis I or meiosis II in the mother
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