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Dextor Dextor
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Posts: 11
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10 years ago
As a genetic counselor, you are visited by two families, each of which has a child with Down syndrome (Trisomy 21).  In Family A, the trisomy 21 child has inherited a 21q21q isochromosome from the mother, who does not have Down syndrome.  The father in this family has a normal karyotype.  In Family B, both parents have a normal karyotype.  What would you tell each family about their risk for bearing another child with Down syndrome?  Explain you reasoning. 
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Answer rejected by topic starter
wrote...
10 years ago
that it is mostly the mother fault that the kid has down syndrome
wrote...
Staff Member
Educator
10 years ago
that it is mostly the mother fault that the kid has down syndrome

Could you provide a better reason? I'm detecting spam here Undecided
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