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(Note, this isn't directly asked in TBR, but a slight variation of what i cam up w/ in trying to identify flaws in my understanding of Punnett Squares)
If Rh-negative mother has a baby w/ heterozygous Rh-positive father, what are the chances that the baby will have erythroblastocis fetalis? Assume, second pregnancy, and Rh antigen to be passed as dominant trait
Possible genotypes for Mom = A(r)A(r), A(r)a
Possible genotypes for Dad = Aa
First off, is this correct representation? (assuming r is super-script, and lower case implies non-carrier of Rh antigen)
Punnett square could look like:
A(r)A(r) A(r)a
----------------------------|------------------------|
Aa | AA(r), AA(r), aA(r), aA(r) | AA(r), Aa, aA(r), aa |
total combinations = 8
EF combinations = 6
% = 6/8 = 75%
If Rh-negative mother has a baby w/ heterozygous Rh-positive father, what are the chances that the baby will have erythroblastocis fetalis? Assume, second pregnancy, and Rh antigen to be passed as dominant trait
Possible genotypes for Mom = A(r)A(r), A(r)a
Possible genotypes for Dad = Aa
First off, is this correct representation? (assuming r is super-script, and lower case implies non-carrier of Rh antigen)
Punnett square could look like:
A(r)A(r) A(r)a
----------------------------|------------------------|
Aa | AA(r), AA(r), aA(r), aA(r) | AA(r), Aa, aA(r), aa |
total combinations = 8
EF combinations = 6
% = 6/8 = 75%