Biology: The Unity and Diversity of Life (MindTap Course List)
14th Edition
ISBN: 9781305073951
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Chapter 14, Problem 5SQ
Summary Introduction
To examine: Whether the statement “A son can inherit an X-linked recessive allele from his father” is true or false.
Introduction: Inheritance patterns determine how a trait is passed from parents to their offspring. They are classified as autosomal or X-linked inheritance and their dominance or recessive.
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X-linked ichthyosis is an X-linked recessive trait that manifests in part as dry, scaly skin (“ichthy-” = fish or fish like). Suppose a couple are considering having a child together. Parent A is heterozygous for the ichthyosis allele while Parent B is hemizygous negative for the ichthyosis allele. What is the probability their child would be unafflicted with ichthyosis but be a carrier of the ichthyosis-causing allele?
a.0%
b.25%
c.50%
d.75%
e.100%
Color-blindness is an X-linked recessive disorder. Under what circumstances will this condition manifest in a child?
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If the child is a male and its mother has the recessive allele
If the child is a female and its father has the recessive allele
If the child is a female and its mother has the recessive allele
If the child is a male and its father has the recessive allele
The allele for color-blindness is carried on the X chromosome. Making color blindness (a recessive trait) an X - linked trait. A colorblind make and a carrier female for color blindness. (But is not colorblind herself) have a child.
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A) what is the % chance that their son will be color blind?
B) what is the % chance that their daughter will be color blind?
Chapter 14 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 14 - Constructing a pedigree is particularly useful...Ch. 14 - Prob. 2SQCh. 14 - Prob. 3SQCh. 14 - Prob. 4SQCh. 14 - Prob. 5SQCh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ______ inheritance....Ch. 14 - A female child inherits one X chromosome from her...Ch. 14 - Prob. 1DAACh. 14 - Prob. 2DAA
Ch. 14 - Prob. 3DAACh. 14 - Prob. 9SQCh. 14 - Expression of the SRY gene on the Y chromosome...Ch. 14 - Prob. 11SQCh. 14 - Prob. 12SQCh. 14 - Prob. 13SQCh. 14 - Prob. 14SQCh. 14 - Match the chromosome terms appropriately. ____...Ch. 14 - Prob. 1GPCh. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes (XX); males...Ch. 14 - A mutated allele responsible for Marfan syndrome...Ch. 14 - The somatic cells of most individuals with Down...Ch. 14 - Mutations in the genes for clotting factor VIII...
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- Please explain why sex linked recessive traits are inherited by the son from his mother. If a mother is a carrier, what percentage of her sons will have the trait? Please give me example of sex linked recessive trait.arrow_forwardAchondroplasia, which is characterized by difficulty converting cartilage to bone and thus results in shortened limbs. This trait is autosomal dominant. (A = achondroplasia allele; a = average height allele.) A husband and wife both have achondroplasia. The couple have a total 12 living children: 6 boys and 6 girls. The husband is colorblind, which is an X-linked recessive trait, and the wife believes there is a chance she is a carrier of colorblindness, since that trait runs in her family. One of the couple’s daughters and three of their sons are colorblind. (Xc = colorblindness allele; XC = normal color vision allele.) A. What are the complete genotypes of the husband and of the wife with respect to both colorblindness AND achondroplasia. Please EXPLAIN your answer. Be sure to indicate which genotype is that of the husband and which is that of the wife.arrow_forwardAchondroplasia, which is characterized by difficulty converting cartilage to bone and thus results in shortened limbs. This trait is autosomal dominant. (A = achondroplasia allele; a = average height allele.) A husband and wife both have achondroplasia. The couple have a total 12 living children: 6 boys and 6 girls. The husband is colorblind, which is an X-linked recessive trait, and the wife believes there is a chance she is a carrier of colorblindness, since that trait runs in her family. One of the couple’s daughters and three of their sons are colorblind. (Xc = colorblindness allele; XC = normal color vision allele.) a) Draw a Punnett square that illustrates the GENOTYPES of all of the children that could be CONCEIVED by this couple. b) What fraction of all of this couple's LIVING/SURVIVING children will have achondroplasia AND simultaneously be colorblind? c)arrow_forward
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