EXAMPLE 2: The parents in the family above produce another son, this time with two Y chromosomes and normal tooth enamel. In which parent did the nondisjunction occur? Explain and/or illustrate. Did nondisjunction occur at meiosis I or II? Explain and/or illustrate.

EXAMPLE 2: The parents in the family above produce another son, this time with two Y chromosomes and normal tooth enamel. In which parent did the nondisjunction occur? Explain and/or illustrate. Did nondisjunction occur at meiosis I or II? Explain and/or illustrate.

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Description: EXAMPLE 2: The parents in the family above produce another son, this time with two Y chromosomes and normal tooth enamel.In which parent did the nondisjunction occur? Explain and/or illustrate.Did nondisjunction occur at meiosis I or II? Explain and/

Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter18: Cell Reproduction

Section: Chapter Questions

Problem 1CT: Normally you cant inherit both copies of a homologous chromosome from the same parent. Why? Assuming...

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Normally you cant inherit both copies of a homologous chromosome from the same parent. Why? Assuming that no crossing over has occurred, how likely is it that one of your non-sex chromosomes is an exact copy of the same chromosome your maternal grandmother had? Explain your answer.
Figure 13.6 Which of the following statements about nondisjunction is true? Nondisjunction only results in gametes with n+1 or n-1 chromosomes. Nondisjunction occurring during meiosis II results in 50 percent normal gametes. Nondisjunction during meiosis I results in 50 percent normal gametes. Nondisjunction always results in four different kinds of gametes.
Compare meiotic anaphase I with meiotic anaphase II. Which meiotic anaphase is most similar to the mitotic anaphase?
A woman who is homozygous for normal color vision mates with a colorblind male. they produce a female child how has only one X chromosome and who is also color blind. In which parent did the nondisjuction take place? Can you specify which meiotic division?
In meiosis, after telophase I, do other cells (comparing one another) have the same combination of genes in each cell? Is it necessary for them to be the same?
Bob has XXY chromosomes (Klinefelter syndrome) and is color blind. His mother and father have normal color vision, but his maternal grandfather is color blind. Assume that Bob’s chromosome abnormality arose from nondisjunction in meiosis. In which parent and in which meiotic division did nondisjunction take place? Assume no crossing over has taken place. Explain your answer.
Explain the process of the following: a. The normal segregation of chromosomes during Meiosis 1 and Meiosis 2 in MALE. b. The abnormal segregation of chromosomes during Meiosis 1 and Meiosis 2 in FEMALE.
In which parent and during which meiotic division did non-disjunction occur? If there is more than one correct answer, list all correct answers. You may assume that non-disjunction occurred in only one parent.
a. If cell division during gametogenesis is non-meiotic, what is its consequence to the future generations of diploid organisms? b. How does non-disjunction in meiosis lead to numerical chromosomal aberration?
In a cell that has just begun the process of meiosis, as shown, what is the probability that a resulting gamete will have only maternally inherited chromosomes? (blue chromosomes are paternally inherited, red are maternally inherited) a) 1/4 b) 1/2 c) 1/8 d) 1/16 e) 1/32
Describe the events taking place during meiosis? What are the different phases? What is the chromosomal content of the final product? Why must this occur to make a chromosomally viable human?
Draw a diagram of Metaphase I and II of meiosis in the father, which illustrates the only possible way in which the father’s chromosomes could have aligned during Metaphase I, and in the subsequent Metaphase II in the same cell, in order to have resulted in the conception of the specific son who has all three of these genetic conditions (achondroplasia, color blindness and deafness).