In humans, a dimple in the chin is a dominant characteristic controlled by a single gene.a. A man who does not have a chin dimple haschildren with a woman with a chin dimple whose mother lacked the dimple. What proportion of theirchildren would be expected to have a chin dimple?b. A man with a chin dimple and a woman who lacksthe dimple produce a child who lacks a dimple.What is the man’s genotype?c. A man with a chin dimple and a nondimpledwoman produce eight children, all having the chindimple. Can you be certain of the man’s genotype?Why or why not? What genotype is more likely,and why?

In humans, a dimple in the chin is a dominant characteristic controlled by a single gene.a. A man who does not have a chin dimple haschildren with a woman with a chin dimple whose mother lacked the dimple. What proportion of theirchildren would be expected to have a chin dimple?b. A man with a chin dimple and a woman who lacksthe dimple produce a child who lacks a dimple.What is the man’s genotype?c. A man with a chin dimple and a nondimpledwoman produce eight children, all having the chindimple. Can you be certain of the man’s genotype?Why or why not? What genotype is more likely,and why?

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Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter19: Introduction To Genetics

Section: Chapter Questions

Problem 5CT: When you decide to breed your Labrador retriever Molly and sell the puppies, you discover that two...

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In humans, a dimple in the chin is a dominant characteristic controlled by a single gene. A man who does not have a chin dimple has children with a woman with a chin dimple whose mother lacked the dimple. What proportion of their children would be expected to have a chin dimple? A man with a chin dimple and a woman who lacks the dimple produce a child who lacks a dimple. What is the man’s genotype? A man with a chin dimple and a non-dimpled woman produce eight children, all having the chin dimple. Can you be certain of the man’s genotype? Why or why not? What genotype is more likely, and why?
Piebald spotting is a condition found in humans in which there are patches of skin that lack pigmentation. The condition results from the inability of pigment-producing cells to migrate properly during development. Two adults with piebald spotting have one child who has this trait and a second child with normal skin pigmentation. a. Is the piebald spotting trait dominant or recessive? What information led you to this answer?
In humans, the genetic disease cystic fibrosis is caused by a recessive allele (a). The normal (healthy) allele is dominant (A). What is the genotype of someone who has cystic fibrosis? What are the two different genotypes that a healthy person could have? If two people were both heterozygous for the cystic fibrosis gene, what fraction of their children would be likely to have this disease? Hint: Draw a Punnett square to figure it out.
Piebald spotting is a condition found in humans inwhich there are patches of skin that lack pigmentation. The condition results from the inability ofpigment-producing cells to migrate properly duringdevelopment. Two adults with piebald spotting haveone child who has this trait and a second child withnormal skin pigmentation.a. Is the piebald spotting trait dominant or recessive?What information led you to this answer?b. What are the genotypes of the parents?
Hair texture is determined by gene c in an incomplete dominance inheritance pattern, where the heterozygous condition (c1c2) results in wavy hair. Hairline is controlled by gene H, where a widow's peak is dominant to a straight hairline. If a woman with curly hair and a straight hairline has a child with a man with a widow's peak and straight hair (his mom had a straight hairline), what is the chance they would have a kid that has exactly the same hair as mom? Draw the Punnett square and demonstrate the possible genotypes and phenotypes that could result from these two parents' mating.
In humans, brown eyes are dominant to blue eyes, and the ability to roll your tongue is dominant to not being able to roll your tongue. If a mother who was heterozygous for eye colour and homozygous recessive for tongue rolling had a baby with a father that was heterozygous for both traits, what is the probability that their child would have blue eyes and could roll their tongue?
In humans, alkaptonuria is a metabolic disorder in which affected persons produce black urine. Alkaptonouria results from an allele (a) that is recessive to the allele for normal metabolism (A). Alana has a normal metabolism, but her brother has alkaptonouria. Alana’s father has alkaptonuria. Give the genotypes of Alana _______, her mother________, her father_______, and her brother______. If Alana’s parents have another child, what is the probability that the child will have alkaptonuria?_____ If Alana marries a man with alkatonuria, what is the probability that their first child will have black urine? _______ What is the probability that 3 of their children will have black urine?__________ If Alana marries a man that does not have alkatonuria, but has a mother that does, then what is the probability that their first child will have black urine? _______ 3 children in a row? ___________
Skin color in humans is determined by polygenic inheritance, which means the more dominant alleles there are, the darker the skin color will be. A medium-toned skinned woman (AaBb) has a child with another medium-toned skinned man (AaBb). What is the probability of them having a very dark-toned skinned child? (Hint: the genotype is homozygous dominant)
In humans, having extra fingers or toes is caused by a dominant allele (E). People with two recessive alleles have 5 fingers and toes on each hand or foot. a. What is the genotype of someone who has 5 fingers and toes on each hand or foot?b. What are the two different genotypes that someone with extra fingers or toes could have?c. If two people both had the normal number of fingers and toes, is there any chance that their children could inherit the allele for extra fingers and toes? Do a Punnett square and show your work.d. If a man who was heterozygous for this gene married someone who was homozygous for the recessive allele, what fraction of their children would you expect to have extra fingers or toes? Do a Punnett square and show your work.
In humans, brown eyes (B) are dominant over blue. A brown eyed man marries a blue-eyed (b) woman and they have three children two of whom are brown-eyed and one of whom is blue-eyed. if blue is recessive, what must the woman’s genotype be?
Both of Ruth's parents have a round face, a dominant trait. Ruth, however, was born with a square face. What does Ruth's phenotype imply about her parents' genes? a. Ruth's parents are both heterozygous when it comes to their facial shape. b. When it comes to facial shape, Ruth's parents gave her one dominant gene and one recessive gene. c. Ruth's parents are both homozygous when it comes to their facial shape. d. Ruth's sister also has a square face.
A study of three generations in a family of a male colleague of the authors indicated that many of the man's blood relatives had died of cardiovascular accidents and coronary heart disease. Others died of other causes but were affected by high blood pressure. What are the implications of this information for the man in question? b. What information and help might a genetic counselor provide?