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BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a mutation in the HEXA gene, r

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Answer #1

1. the III 3 is the carrier for disease - Tt (heterozygous)

2. the III 2 is normal - TT ( homozygous dominant)

the probability that their child will have Tay-Sachs which is the homozygous recessive disorder = tt

T t
T TT Tt
T TT Tt

so according to Punnett square

  • the child will have Tay-Sachs ( tt) = 0 %
  • the child with carrier = 50 %
  • normal child = 50 %
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