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Biology, 14.10.2019 19:30 Apple557

Agenetics question: tay-sachs disease is a rare human disease in which toxic substances accumulate in nerve cells. the recessive allele is inherited in a simple mendelian manner. a woman is planning to marry her first cousin, but the couple discovers that their shared grandfather's sister died in infancy of tay-sachs disease.

what is the probability that the cousins' first child will have tay-sachs disease, assuming that all people who marry into the family are homozygous normal?

i'll draw the pedigree i have and the work i've done - can't seem to get the right answer, though.

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