ESSENTIALS OF GENETICS-MODIFIED ACCESS
9th Edition
ISBN: 9780134190006
Author: KLUG
Publisher: PEARSON
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Chapter 6, Problem 23PDQ
A boy with Klinefelter syndrome (47, XXY) is born to a mother who is phenotypically normal and a father who has the X-linked skin condition called anhidrotic ectodermal dysplasia. The mother's skin is completely normal with no signs of the skin abnormality. In contrast, her son has patches of normal skin and patches of abnormal skin. (a) Which parent contributed the abnormal gamete? (b) Using the appropriate genetic terminology, describe the meiotic mistake that occurred. Be sure to indicate in which division the mistake occurred. (c) Using the appropriate genetic terminology, explain the son's skin
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A boy with Klinefelter syndrome (47,XXY) is born to a motherwho is phenotypically normal and a father who has the X-linkedskin condition called anhidrotic ectodermal dysplasia. The mother’sskin is completely normal with no signs of the skin abnormality.In contrast, her son has patches of normal skin and patchesof abnormal skin.
Question: Which parent contributed the abnormal gamete?
Hemophilia is another example of an X-linked disease caused when a recessive allele (Xh) is expressed. If a normal male reproduces with a heterozygous normal female, what are the expected genotypes and phenotypes? Will any of their daughters develop hemophilia?
Why doesn’t the father (II-1) have the disease breast cancer?
What is the formal name for an individual having the gene but not showing the trait?
Chapter 6 Solutions
ESSENTIALS OF GENETICS-MODIFIED ACCESS
Ch. 6 - CASE STUDY| Fish tales Aquatic vegetation...Ch. 6 - CASE STUDY |Fish tales Aquatic vegetation...Ch. 6 - CASE STUDY |Fish tales
Aquatic vegetation...Ch. 6 - HOW DO WE KNOW? In this chapter, we focused on...Ch. 6 -
CONCEPT QUESTION
2. Review the Chapter Concepts...Ch. 6 -
3. Define these pairs of terms, and distinguish...Ch. 6 -
4. For a species with a diploid number of 18,...Ch. 6 - What explanation has been proposed to explain why...Ch. 6 - Contrast the fertility of an allotetraploid with...Ch. 6 -
7. Why do human monosomies most often fail to...
Ch. 6 -
8. Describe the origin of cultivated American...Ch. 6 - Predict how the synaptic configurations of...Ch. 6 - Inversions are said to “suppress crossing over.”...Ch. 6 -
11. Predict the genetic composition of gametes...Ch. 6 - Human adult hemoglobin is a tetramer containing...Ch. 6 -
13. The primrose, Primula kewensis, has 36...Ch. 6 - Certain varieties of chrysanthemums contain 18,...Ch. 6 - Drosophila may be monosomic for chromosome 4, yet...Ch. 6 - Mendelian ratios are modified in crosses involving...Ch. 6 -
17. Having correctly established the F2 ratio in...Ch. 6 -
18. In a cross between two varieties of corn,...Ch. 6 -
19. A couple planning their family are aware that...Ch. 6 -
20. A woman who sought genetic counseling is...Ch. 6 - The woman in Problem 20 has had two miscarriages....Ch. 6 -
22. In a recent cytogenetic study on 1021 cases...Ch. 6 -
23. A boy with Klinefelter syndrome (47,XXY) is...Ch. 6 - In a human genetic study, a family with five...Ch. 6 - A 3-year-old child exhibited some early indication...Ch. 6 - A normal female is discovered with 45 chromosomes,...
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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 autosomal (not X-linked) gene for brachydactyly, short fingers, is dominant to normal finger length. Assume that a female with brachydactyly in the heterozygous condition is married to a man with normal fingers. What is the probability that(a) their first child will have brachydactyly?(b) their first two children will have brachydactyly?(c) their first child will be a brachydactylous girl?arrow_forwardA color-blind man marries a woman with normal vision whose father was color-blind. Remember that color-blindness is an X-linked recessive trait. Hint: see figure 12.7 in book. A) What is the probability that their first child will be a color-blind daughter? B) What is the probability that their first son will be color-blind?arrow_forwardWhy does a single X chromosome cause infertility and other abnormalities in Turner Syndrome subjects?arrow_forward
- Duchenne muscular dystrophy (DMD), marked by muscular degeneration, results from an X- linked recessive gene. Thus, a female who is heterozygous for this gene and does not have the disease can be a carrier. What kind of offspring can you expect from a DMD-affected male and a carrier female? Can there be a carrier male?arrow_forwardCould a woman who expresses the x-linked color-blind trait have a son with normal vision?arrow_forwardA karyotype shows that a child has Klinefelter syndrome (47,XXY). If the child is also colorblind (due to a recessive X-linked allele), despite his parents having normal color vision, in which parent and stage of meiosis did nondisjunction occur? And explain why .arrow_forward
- A boy with Klinefelter syndrome (47,XXY) is born to a motherwho is phenotypically normal and a father who has the X-linkedskin condition called anhidrotic ectodermal dysplasia. The mother’sskin is completely normal with no signs of the skin abnormality.In contrast, her son has patches of normal skin and patchesof abnormal skin. Using the appropriate genetic terminology, explain theson’s skin phenotype.arrow_forwardCan a son be a carrier for an X-linked trait? Explain.arrow_forwardI will be adding two questions here because I asked two of the same questions twice by accident earlier. A man and a woman do not have hemophilioa, but the womans father did. (Hemophilia is X-linked recessive). a) What is the probability that they will have a child with hemophilia? b) Is it possible for any of their daughters to be affected? Explain. A cross between a horse homozygous for red hair and a horse homozygous for white hair results in offspring with the coat colour called roan. When you look at the fur of the roan offspring you see both red and white hairs. What type of inheritance best explains this? a) blending inheritance b)codominance c)incomplete codominance d)multiple allelesarrow_forward
- Chands syndrome is an autosomal recessive condition characterized by very curly hair, underdeveloped nails, and abnormally shaped eyelids. In the pedigree below: Which individuals must be carriers (heterozygotes)? ----- arrow_forwardDuchenne muscular dystrophy is an X-linked, recessive disorder in which muscles waste away early in life, resulting in death in the teens or twenties. A man and woman in their late thirties have five children—three boys (ages 1, 3, and 10 years) and two girls (ages 5 and 7 years). The oldest, boy shows symptoms of the disease. What are the probabilities that their other children will develop the disease? Give only typing answer with explanation and conclusionarrow_forwardwhich Genotype below is considered a carrier for an x-linked recessive disorder?arrow_forward
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