humans, dark hair (D) is dominant over blondness (d), and color blindness (c) is a sex-linked recessive trait. A woman has a blond brother, a blond mother, and a dark-haired father. Her brother and her parents have normal vision. She bears the following three children by her blond, normal-visioned husband: a dark-haired son with normal vision, a dark-haired daughter with normal vision, and a dark-haired color blind son. Make a pedigree of the entire family showing the probable genotypes of all individuals.

humans, dark hair (D) is dominant over blondness (d), and color blindness (c) is a sex-linked recessive trait. A woman has a blond brother, a blond mother, and a dark-haired father. Her brother and her parents have normal vision. She bears the following three children by her blond, normal-visioned husband: a dark-haired son with normal vision, a dark-haired daughter with normal vision, and a dark-haired color blind son. Make a pedigree of the entire family showing the probable genotypes of all individuals.

Concepts of Biology

1st Edition

ISBN:9781938168116

Author:Samantha Fowler, Rebecca Roush, James Wise

Publisher:Samantha Fowler, Rebecca Roush, James Wise

Chapter8: Patterns Of Inheritance

Section: Chapter Questions

Problem 17CTQ: Can a male be a carrier of red-green color blindness?

See similar textbooks

Similar questions

In humans, dark hair (D) is dominant over blondness (d), and color blindness (c) is a sex-linked recessive trait. A woman has a blond brother, a blond mother, and a dark-haired father. Her brother and her parents have normal vision. She bears the following three children by her blond, normal-visioned husband: a dark-haired son with normal vision, a dark-haired daughter with normal vision, and a dark-haired color blind son. What is the probability that her next (fourth) child will be a colorblind boy.
In humans, dark hair (D) is dominant over blondness (d), and color blindness (c) is a sex-linked recessive trait. A woman has a blond brother, a blond mother, and a dark-haired father. Her brother and her parents have normal vision. She bears the following three children by her blond, normal-visioned husband: a dark-haired son with normal vision, a dark-haired daughter with normal vision, and a dark-haired color blind son. If he is a colorblind boy, what is the probability that he will have dark hair?
In humans, the gene for albinism (a) is recessive to the gene for normal skin pigmentation (A). If two heterozygous persons have children, what is the probability they will have a child who is an albino? What is the probability they will have a child that is a carrier of the recessive gene?
In human beings, the gene for red‑green colorblindness (r) is sex‑linked and recessive to its allele for normal vision (R), while the gene for freckles (F) is autosomal and dominant over its allele for nonfreckled (f). A nonfreckled, normal‑visioned woman whose father was freckled and colorblind, marries a freckled, colorblind man whose mother was nonfreckled. What is the genotype of the woman's father? What is the probability that the couple's first child will be a non-freckled, normal visioned girl? What is the probability that the first two children born to the couple will be freckled and colorblind girls?
Both red/green color blindness (R=normal, r=colorblind) and Duchenne-type muscular dystrophy (D=normal, d=muscular dystrophy) are X-linked recessive traits that map close to each other. A woman has a father who is red/green color blind. Her mother's family has a history of Duchenne's muscular dystrophy. This woman is apparently healthy with neither color blindness nor muscular dystrophy. She marries a healthy man and they have four sons and two daughters. Half the sons are healthy but color blind, the other half have normal color vision, but have Duchenne's muscular dystrophy. The daughters are both normal. What is the genotype of the woman? ** The notation is written as X/X (so the / separates the two X chromosomes in a female) Group of answer choices RD/rd rd/rd Rd/rD RD/RD
In human beings, the gene for red‑green colorblindness (r) is sex‑linked and recessive to its allele for normal vision (R), while the gene for freckles (F) is autosomal and dominant over its allele for nonfreckled (f). A nonfreckled, normal‑visioned woman whose father was freckled and colorblind, marries a freckled, colorblind man whose mother was nonfreckled. What is the probability that the first child born to the couple will either be a freckled, colorblind boy or a non‑freckled, normal visioned girl or a non-freckled, normal visioned boy? What is the probability that the first four children born to the couple will be freckled and normal visioned girls?
A man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive. a) How many of their daughters might be expected to be color-blind dwarfs? b)What proportion of their sons would be color-blind and of normal height? c)They have a daughter who is a dwarf with normal color vision. What is the probability that she is heterozygous for both genes?
Colour-blindness is the result of an X-linked recessive allele, Xc. The allele for normal eyesight is XC. (a) A woman with normal colour vision whose father was colour-blind marries a colour-blind man. Give the genotypes and phenotypes of their children. What ratio of their children can be expected to be colour-blind? (b) A man with normal colour vision whose father was colour-blind marries a woman carrier of the colour-blind allele. What is the likelihood that their children will be colour-blind? Carriers of the trait?
In humans, one type of red-green colorblindness (n) is sex-linked and recessive. A) A woman who is a carrier marries a man with normal vision. What is the chance of having color-blind daughters? Color-blind sons? B) A heterozygous woman and a color-blind man marry. What is the chance of having color-blind daughters? Color-blind sons?
A woman without red-green colorblindness and with a normal chin, whose mother was colorblind, marries a cleft-chinned, non-colorblind man whose mother had a normal chin. Recall that red-green colorblindness is sex-linked recessive, but mid-chin fissure (cleft) is autosomal dominant. What are the expected phenotypic ratios of the children? Show your work.
My father is homozygous dominant (T) for tall and (B) black hair. My mother is heterozygous recessive (t) and (b) brown hair. What are the possible genotypes and phenotypes? Circle all the genotypes.
A man who is a dwarf due to achondroplasia and has normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplasia is autosomal dominant, and red-green color blindness is X-linked recessive. What are the possible genotypes and phenotypes of their children? What are the ratios for each?