For a recessive condition, two normal heterozygous individuals have children. What is the likelihood of their children being affected by this condition? What is the likelihood of their children being carriers without the condition? What is the likelihood of their asymptomatic children being carriers? Suppose that an individual with the condition has children with a heterozygous individual, what is the likelihood of their children being carriers?

Freckles is determined by a single gene and having freckles is dominant over not having freckles. If a man with freckles and a woman without freckles have a child that does not have freckles then a)the man is heterozygous for the freckles gene. b)the child is heterozygous for the freckles gene. c)the woman and man are both heterozygous for the freckles gene. d) the woman is heterozygous for the freckles gen

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?

In humans, albinism (lack of skin pigment) is an autosomal recessive trait. The first child of two normally pigmented parents is an albino. Which of the following is true about this family? SELECT ALL THAT ARE CORRECT. A) Their first child (described above) has a homozygous recessive genotype B) The next child born to this couple has a 25% chance of being albino. C) If the next child born to this couple is male, he has a greater chance of being albino. D) The parents are both heterozygous for albinism. E) The probability of their second child being albino is 0% F) If the second and third child born to this couple are albino, the fourth child has 100% chance of also being albino.

The three genes X, Y, and Z are linked on an autosomal chromosome in humans (X to Y is 15 cM, and Y to Z is 18 cM). If an individual that is heterozygous at all three loci (XYZ/xyz) has children with an individual that is homozygous recessive at all three loci (xyz/xyz), what is the probability that they will have a child that is phenotypically identical to either parent (X-Y-Z- or xxyyzz)? Assume there is no genetic interference to double crossover events at this site.

An unaffected woman for a human disorder marries and unaffected man and they have children. This results in 3 affected sons, and one unaffected daughter, which ends up having children later on with an unaffected man and has 2 affected sons. A) Draw a simple pedigree diagram for this family, including a legend. B) What is the likely mode of inheritance of this trait: Please explain C) Provide the genotypes of the original mother and the daughter. Use a capital letter for the dominant allele and lowercase letter for the recessive allele. D) If one of the affected sons from the original marriage marries a 2nd cousin that is a carrier of this trait and has children, what is the probability that they will have 3 affected sons?

In humans, blue eyes are inherited as a recessive autosomal trait and color blindness is an X-linked recessive trait.  A woman with blue eyes and normal color vision (her father was colorblind) marries a man who has normal color vision.  The man has brown eyes, but his mother had blue eyes.  What is the probability that this couple will have a child with normal vision and blue eyes?