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Galactosemia is an autosomal recessive human disorder that affects 1/250,000 individuals in Sweden. Individuals with galactosemia have genotype “gg”. What is the frequency of heterozygous individuals in this population? Answer 0.000004 0.002 0.004 0.996 0.998
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I don't know what I'm doing, someone please help me out again @Abhisar last question!
is answer known ?
what do you mean?
do u know the answer of this question ?
nope.
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not sure about this one..!! :(
Yea, I'm having a tough time also can you @ people who might know. @alphadxg is offline :( he helped me with 2 yesturday like this
no body else seems to be online this time
|dw:1401596460599:dw| |dw:1401596496133:dw|
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