Biology

Biology, 20.07.2019 04:30, Tyjon16

Aman who has normal hearing and has a recessive deafness allele on chromosome 17 marries a woman who also has normal hearing and also has a recessive deafness allele, but this allele is on chromosome 3. the probability that their children will be deaf due to either of these mutated genes is closest to

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Biology, 27.07.2019 09:30, Soloved

Sue has normal hearing but her sister suffers from deafness determined by a rare recessive allele. what is the probability that sue's phenotypically normal daughter is heterozygous for the gene? (hint: the word "rare" implies that the recessive allele is not frequent in the population; you can assume that the father of sue's daughter is not likely a carrier)

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Biology, 19.09.2019 20:10, 910190hps

Aman and a woman are both deaf due to being homozygous for a recessive autosomal mutant allele. however, they are homozygous recessive at different gene loci. if all their children have normal hearing, which event has occurred within each child?

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Biology, 05.10.2019 00:20, danielahchf

In humans, a type of blindness is due to a dominant allele; normal vision is the result of a recessive allele. migraine headaches are due to a dominant allele, and normal (no headaches) is recessive. a male who is heterozygous for blindness and does not suffer from headaches marries a woman who has normal vision and does not suffer from migraines. could they produce a child with normal vision who does not suffer from headaches? if yes, can the probability of such a child be determined?

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Social Studies, 07.10.2019 18:10, moraleskarina491

Dr. smith's parents have normal hearing. however, dr. smith has an inherited form of deafness. deafness is a recessive trait that is associated with the abnormal allele d. the normal allele at this locus, associated with normal hearing, is d. dr. smith's parents could have which of the following genotypes?

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