an autosomal recessive disease is whrn two copies of an abnormal gene must be present in order for the disease to be seen. so if the parwnts are not affected they must be heterozygous.
for the first child born to a couple who both carry the gene (but do not have signs of disease), the expected outcome for each pregnancy is:
If a couple with the genotypes FfEeWwHhDd and FfEeWwHhDd has children, what is the chance the...
a. Determine the most probable mode of inheritance: autosomal or sex-linked, dominant or recessive, of the disorders in the two pedigrees shown below and indicate the genotypes of as many individuals as possible. 0 0 | ●ㅇ 이 vod 0d b. If individual IV-1 from the first pedigree marries an affected woman, what is the probability that their first child is affected by the disorder? c. If individual IV-3 from the second pedigree marries a normal man, what is the...
A couple has three children. Assuming each child has an equal chance of being a boy or a girl, what is the probability that they have at least one girl? a. .125 b. .5 c. 1 d. .875
A couple has two children and the oldest child is a boy. If the probabilities of having a boy or girl are both equal what is the probability that the couple has 2 boys
Suppose that you are studying is a rare recessive condition in humans whereby affected individuals are unable to metabolize a sugar found in certain foods. A woman and her husband are both heterozygous for the allele causing the condition. A) If the woman is pregnant with twins and the twins are dizygotic (non-identical), what is the probability that both twins will be girls and be affected? B) What is the probability if the girl twins are identical (monozygotic) and both...
A couple of normal ancestry has two normal children and an infant affected with sickle cell anemia. The sister of the husband wants to marry the brother of the wife. In such a mating, what would be the probability of their first child having sickle cell anemia?
1. For each of the following blood types, list the possible genotypes: Phenotype Possible Genotypes A B AB O 2. Dr. Paul is blood type O. His father was blood type A and his mother was blood type B. What were the genotypes of his parents? What are the possible blood types and phenotypic ratios expected for a cross involving these parental genotypes? 3. In the ABO blood system in human beings, alleles A and B are codominant and both are...
모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic disorder is segregating. 3. Each of the pedigrees shown represents a human family within which a genetic disorder is se Assume the two traits are extremely rare in the population and completely penetrant. Part 1. For the first pedigree. lisorder: autosomal recessive, autosomal a. Determine the most probable inheritance pattern of the disorder: autosomal recessive dominant, X-linked recessive or X-linked dominant. b. Indicate the...
6. 11-5 and 1-6 meet while attending a lecture concerning a rare metabolic disease. They each have at least one sibling who has the disease. What is the probable mode of inheritance for this disease? 1l-5 and I-6 fall in love but are apprehensive about having children since they know that the chance of their first child having the disease is increased. What is the probability that one of their children will inherit the disorder? English (United States) age 3...
A rare X linked disease runs on both sides of the families from a prospective couple. Susana's brother as well as Joe's father have the condition. What is the probability that Susana and Joe's first child has the disease? Select one: a. 2/18 b. 1/4 c. 2/3 O d. 1/8 e. 1/16
1. A dimpled woman wants to have children and finds a suitable donor at her local sperm bank. Her genotype is Dd, and her chosen sperm donor’s genotype is dd. Her plan is to produce 3 children, and she is curious to know the probability that she will have at least two children with dimples. That probability is: 2. A dimpled woman wants to have children and finds a suitable donor at her local sperm bank. Her genotype is Dd,...