phenylketonuria is an inherites disease caused by a recessive allele. is a women and her husband who are both carriers, have a child, what is the probability of having a child that does not express pku?

Question

15-12-2022
Biology

Answered

phenylketonuria is an inherites disease caused by a recessive allele. is a women and her husband who are both carriers, have a child, what is the probability of having a child that does not express pku?

Answer :

Other Questions

In domesticated dogs, hair type is controlled by two different alleles. The allele for wire hair is (h) and the allele for smooth hair is (h). When two heterozy

Pooja has green eyes while her parents and brother have black eyes. Pooja’s husband Ravi has black eyes whil his mother has green eyes and his father has black

what is the probability of albinism in the offspring of a cross between two mice with aabb alleles?

Which of these is the best reason for nina to monitor her bank account statements online or on her cell phone app? to know when her bills are due to determine t

1 how did there get to be such a wide variety of life 2 what does the statement extinction and speciation are both part of evolution 3 why do scientists who stu

In both eukaryotes and prokaryotes, gene expression is primarily regulated at the level of?

Fossils of the same life form species have been found on continents that are now divided by oceans. in one to two sentences, explain how this could be possible

Drag each tile to the correct location on the diagram. Sort the attributes based on whether they describe only Earth, only Mars, or both Earth and Mars. has liq

What are some examples of organisms that are difficult to classify or have been reclassified based on new evidence?

AnnuG AnnuG · Answer 1 · 2022-12-19T12:29:07-05:00

The probability of having a child that does not express PKU when the women and her husband both are carriers will be 25 %.

PKU is a genetic disease where the levels of phenylketonuria are high in the blood of the affected person. This happens due to the mutation in the phenylalanine hydroxylase (PAH) gene. The gene is responsible for the breakdown of the phenylalanine in the body.

Carriers are the heterozygous individuals that carry one dominant and one recessive allele for the trait. When two heterozygous individuals cross the probability of offspring having homozygous recessive or dominant genotype is 25 % for each. While the probability of obtaining heterozygotes is 50%.

To know more about PKU, here

brainly.com/question/13954156

#SPJ4