Tay-Sachs disease is inherited as an autosomal recessive trait and is lethal in the homozygous recessive...

Tay-Sachs disease is inherited as an autosomal recessive trait and is lethal in the homozygous recessive condition at the age of 2years. A heterozygote marries a genotypically normal individual. What is the probability of having children that have Tay-Sachs?

Solutions

Expert Solution

Please hit on the like button if you are satisfied with the answer. Give comments for further clarification/assistance. Thanks! Have a good day.

gladiator answered 1 year ago

Next > < Previous

Related Solutions

1. A severe disease that is inherited as an autosomal recessive trait is more likely to...

1. A severe disease that is inherited as an autosomal recessive trait is more likely to skip generations in a pedigree than an autosomal recessive trait that cuases a harmless phenotypic variant because a) all autosomal recessive traits skip generations b) a person with the harmless variant is less likely to reproduce than a person with the disease c) a person with an autosomal recessive disease is less likely to be well enough to reproduce than a person with a...

Assume that a bi-allelic locus controls a (a) codominant trait, and (b) homozygous recessive lethal trait....

Assume that a bi-allelic locus controls a (a) codominant trait, and (b) homozygous recessive lethal trait. Show a Mendelian monohybrid intercross, and the expected phenotypic ratios in the F2 in each case.

Tay-Sachs is an autosomal recessive disorder that results in progressive loss of brain tissue Jewish settlers...

Tay-Sachs is an autosomal recessive disorder that results in progressive loss of brain tissue Jewish settlers and is engaged to Howard. Maria and Howard are concerned about having children since one of Maria’s uncles on her mother’s side had died from Tay Sachs. Howard’s family is of Scandinavian origin has no record of Tay Sach. You are asked to advise Maria and Howard as to the risk of them having a child with Tay Sachs. (FYI, the incidence of Tay...

Tay Sachs is an autosomal recessive disease's leading to nerve cell damage and early childhood death....

Tay Sachs is an autosomal recessive disease's leading to nerve cell damage and early childhood death. 1 in 250 humans are carriers. There is NO BENEFIT to being a carrier for this disease. Since there is no benefit, list the hardy Weinberg assumptions in order of likely reasons that this disease is so widespread AND describe why you piked this order. (no more than 1-2 sentences each)

HUNTINGTON’S DISEASE is an autosomal dominantly inherited, degenerative human disease of the nervous system. Individuals homozygous...

HUNTINGTON’S DISEASE is an autosomal dominantly inherited, degenerative human disease of the nervous system. Individuals homozygous for this dominant gene almost always die as a fetus. The disease has no obvious phenotypic effects in a heterozygous individual, until a person is about 35-40 years old, well into child-rearing years. There is no known cure for this genetic disease. E. Determine the results of a mating between two parents, both of whom will get Huntington’s disease. Provide the Punnett square and...

Suppose colourblindness is an X-linked recessive trait, while Huntington's disease is an autosomal dominant trait. Assume...

Suppose colourblindness is an X-linked recessive trait, while Huntington's disease is an autosomal dominant trait. Assume both traits are rare. A colourblind man decides to have children with a women who is heterozygous for both genes. What is the probability that they will have a child that is colourblind and does not have Huntington's?

If an X-linked recessive trait was lethal to the development of an embryo, answer the following...

If an X-linked recessive trait was lethal to the development of an embryo, answer the following questions: A. could carrier females pass this trait to sons that survive child birth? B. could carrier females pass this trait to daughters that survive child birth? C. could fathers pass this trait to daughters that survive child birth? D. could fathers pass this trait to sons that survive child birth?

If 4% of a population has an autosomal recessive trait, what portion of the population are...

If 4% of a population has an autosomal recessive trait, what portion of the population are likely to be carriers? Assume that the population is large, and that the recessive trait doesn't affect fitness of the individual. List your answer as a percentage.

Albinism is a rare autosomal recessive trait in which there is a complete absence of melanin...

Albinism is a rare autosomal recessive trait in which there is a complete absence of melanin pigment in the skin, eyes, and hair. A normally pigmented woman whose parents are normal has a brother who is albino. She marries a normally pigmented man whose grandfather was albino. What is the probability their first child will be albino? I would like to see the problem worked out. Dont understand why it is 1/12. Thank you in advance

1- When crossing two organisms for a single trait - one that is homozygous recessive with...

1- When crossing two organisms for a single trait - one that is homozygous recessive with one that is homozygous dominant - what is the chance of producing an offspring with the homozygous recessive phenotype? Group of answer choices )% 75% 25% 100% 2- Incomplete dominance is when? Group of answer choices Homozygotes show an intermediate phenotype There is no homozygous genotype Heterozygotes show an intermediate phenotype Heterozygotes share dominance 3- When antibodies in the plasma attach to antigens on...

Subjects