Anatomy & Physiology: The Unity of Form and Function (Standalone Book)
7th Edition
ISBN: 9780073403717
Author: Kenneth S. Saladin Dr.
Publisher: McGraw-Hill Education
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Textbook Question
Chapter 29, Problem 5TYR
Which of these results from aneuploidy?
- a. Turner syndrome
- b. fetal alcohol syndrome
- c. nondisjunction
- d. progeria
- e. rubella
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Which of these results from aneuploidy?a. Turner syndromeb. fetal alcohol syndromec. nondisjunctiond. progeriae. rubella
오오토오 오모
a. What is the mode of inheritance for this rare disease?
b. What is the genotype of the following (in cases where the genotype is uncertain, list all
possible genotypes.)
i.
1.1
ii.
1.2
ii.
II.1
iv.
I1.4
C. What is the likelihood that II.3 will have a child that is a carrier?
d.
What is the likelihood that II.2 has three affected children?
A man who is color blind and has hemophilia and a woman who is neither color blind nor a hemophiliac have a daughter with triple X syndrome (XXX) who has hemophilia and is color blind. Where did the nondisjunction occur?
Group of answer choices
a. Paternal meiosis II only
b. Maternal meiosis II or paternal meiosis I
c. Maternal meiosis I or paternal meiosis II
d. Paternal meiosis II or maternal meiosis II
e. Maternal meiosis II only
(b is not the right answer)
Chapter 29 Solutions
Anatomy & Physiology: The Unity of Form and Function (Standalone Book)
Ch. 29.1 - Prob. 1BYGOCh. 29.1 - Prob. 2BYGOCh. 29.1 - Prob. 3BYGOCh. 29.1 - Prob. 4BYGOCh. 29.1 - Prob. 1AYLOCh. 29.1 - Prob. 2AYLOCh. 29.1 - Prob. 3AYLOCh. 29.1 - Prob. 4AYLOCh. 29.1 - Prob. 5AYLOCh. 29.1 - Prob. 6AYLO
Ch. 29.1 - Prob. 7AYLOCh. 29.1 - Prob. 8AYLOCh. 29.1 - Prob. 9AYLOCh. 29.1 - Prob. 10AYLOCh. 29.1 - Prob. 11AYLOCh. 29.2 - Prob. 5BYGOCh. 29.2 - Prob. 6BYGOCh. 29.2 - Prob. 7BYGOCh. 29.2 - Prob. 8BYGOCh. 29.2 - Prob. 9BYGOCh. 29.2 - Prob. 1AYLOCh. 29.2 - Prob. 2AYLOCh. 29.2 - Prob. 3AYLOCh. 29.2 - Prob. 4AYLOCh. 29.2 - Prob. 5AYLOCh. 29.2 - Prob. 6AYLOCh. 29.2 - Prob. 7AYLOCh. 29.2 - Prob. 8AYLOCh. 29.2 - Prob. 9AYLOCh. 29.2 - Prob. 10AYLOCh. 29.2 - Prob. 11AYLOCh. 29.3 - Prob. 10BYGOCh. 29.3 - Prob. 11BYGOCh. 29.3 - Prob. 12BYGOCh. 29.3 - Prob. 1AYLOCh. 29.3 - Prob. 2AYLOCh. 29.3 - Prob. 3AYLOCh. 29.3 - Prob. 4AYLOCh. 29.3 - Prob. 5AYLOCh. 29.3 - Prob. 6AYLOCh. 29.3 - Prob. 7AYLOCh. 29.3 - Prob. 8AYLOCh. 29.3 - Prob. 9AYLOCh. 29.3 - Prob. 10AYLOCh. 29.3 - Prob. 11AYLOCh. 29.4 - Prob. 13BYGOCh. 29.4 - Prob. 14BYGOCh. 29.4 - Prob. 15BYGOCh. 29.4 - Prob. 16BYGOCh. 29.4 - Prob. 17BYGOCh. 29.4 - Prob. 1AYLOCh. 29.4 - Prob. 2AYLOCh. 29.4 - Prob. 3AYLOCh. 29.4 - Prob. 4AYLOCh. 29.4 - Prob. 5AYLOCh. 29.4 - Prob. 6AYLOCh. 29.4 - Prob. 7AYLOCh. 29.4 - Prob. 8AYLOCh. 29.4 - Prob. 9AYLOCh. 29.4 - Prob. 10AYLOCh. 29.4 - Prob. 11AYLOCh. 29.4 - Prob. 12AYLOCh. 29.4 - Prob. 13AYLOCh. 29.4 - Prob. 14AYLOCh. 29.4 - Prob. 15AYLOCh. 29.4 - Prob. 16AYLOCh. 29.4 - Prob. 17AYLOCh. 29.4 - Prob. 18AYLOCh. 29.4 - Prob. 19AYLOCh. 29 - Prob. 1TYRCh. 29 - Prob. 2TYRCh. 29 - Prob. 3TYRCh. 29 - Prob. 4TYRCh. 29 - Which of these results from aneuploidy? a. Turner...Ch. 29 - Fetal urine accumulates in the ______ and...Ch. 29 - One theory of senescence is that it results from a...Ch. 29 - Prob. 8TYRCh. 29 - Prob. 9TYRCh. 29 - Prob. 10TYRCh. 29 - Prob. 11TYRCh. 29 - Aneuploidy is caused by _____, the failure of two...Ch. 29 - Prob. 13TYRCh. 29 - Prob. 14TYRCh. 29 - Prob. 15TYRCh. 29 - Prob. 16TYRCh. 29 - Prob. 17TYRCh. 29 - Prob. 18TYRCh. 29 - Prob. 19TYRCh. 29 - Prob. 20TYRCh. 29 - Prob. 1BYMVCh. 29 - Prob. 2BYMVCh. 29 - Prob. 3BYMVCh. 29 - Prob. 4BYMVCh. 29 - Prob. 5BYMVCh. 29 - Prob. 6BYMVCh. 29 - Prob. 7BYMVCh. 29 - Prob. 8BYMVCh. 29 - Prob. 9BYMVCh. 29 - Prob. 10BYMVCh. 29 - Prob. 1TFCh. 29 - Prob. 2TFCh. 29 - Prob. 3TFCh. 29 - Prob. 4TFCh. 29 - Prob. 5TFCh. 29 - Prob. 6TFCh. 29 - Prob. 7TFCh. 29 - Prob. 8TFCh. 29 - Prob. 9TFCh. 29 - Prob. 10TFCh. 29 - Suppose a woman had a mutation resulting in a...Ch. 29 - Prob. 2TYCCh. 29 - Prob. 3TYCCh. 29 - Prob. 4TYCCh. 29 - Only one sperm is needed to fertilize an egg, yet...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- The genotype XXY corresponds to: a. Klinefelter syndrome b. Turner syndrome c. Tripto-X d. Jacob syndromearrow_forwardvon Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardWhich of the following can be identified by anabnormal karyotype?a. Sickle cell diseaseb. Cystic fibrosisc. Monosomy Xd. Tay-Sachs diseasee. Huntington’s choreaarrow_forward
- What is it called when chromosomes fail to separate properly during meiosis? A. Nondisjunction B. Karyotype C. Chromosomal separation failure D. Inappropriate separation E. Karyokinesisarrow_forwardIn terms of ontigeny, differentiate the following; A. Epiphysis from hypophysis B. Retina from organ of Cortiarrow_forwardJoe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for this disease from the following people? Yes No a. His mother's mother b. His mother's father c. His father's mother d. His father's fatherarrow_forward
- Colorblindness is a recessive x-linked trait. Which genotype represents a male with normal vision? a. XNXN b. XYN c. XnY d. XNYarrow_forwardidentify if it is True or False 1. ABO Blood Group show codominance. 2. Alleles are different forms of genes. 3. Sex-linked inheritance means that only the X-chromosomes are affected. 4. The carriers of hereditary materials are the genes. 5. Hemophilia is a sex-linked trait.arrow_forwardA boy is color-blind (X-linked recessive) and has a straight hairline (autosomal recessive). Which could be the genotype of his mother? Select one: А. Вbxwxw B. Bbww C. Xbxbww D. Xbywwarrow_forward
- While studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this sign was founded only in the men and it was inherited from father to the son. Define the type of hypertrichosis inheritance? Select one: a. Y-linked b. Autosomal-recessive O c. Autosomal-dominant d. Recessive, X-linked e. Dominant, X-linkedarrow_forwardWhen we say that a woman is a carrier for a genetic disease or disorder it means that a. she can pass the gene only to male children b. she has 1 gene, but not the disorder c. she can pass the gene only to female children d. she has 2 genes for the disorderarrow_forwardWhy must males inherit colorblindness or hemophilia from their mothers? I. Male offspring inherit the Y chromosome from their father II.Y chromosome of male offspring does not carry the aforementioned sex-linked trait III.X chromosome of male offspring carries the aforementioned sex-linked trait IV.Sex-linked traits are passed on from the double X chromosomes of the mothers. * I, IV I, II I, II, III I, II, III, IVarrow_forward
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