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Biology 12 Online
OpenStudy (anonymous):

Huntington's disease is a genetic disorder that can result in memory loss and abnormal body movements. Huntington's disease results from a defective gene (H) that is dominant to the allele that produces normal function (h). This means that... I. if someone is heterozygous for Huntington's disease, then he/she will be a carrier but will not have the disease. II. if a child has Huntington's disease, then at least one of his/her parents has the disease. III. if two parents do not have Huntington's disease, then their children will not have the disease. I and III only II and III onl

OpenStudy (anonymous):

I and III only II and III only I, II, and III III only

OpenStudy (shadeyghost):

ok, which do you think it is?

OpenStudy (shadeyghost):

ok, I can't be correct because if you are heterozygous for a particular trait, that means that you have Hh, so you have the disease

OpenStudy (shadeyghost):

@epicjellypanda hello?

OpenStudy (anonymous):

I'm sorry, computer problems @shadeyghost

OpenStudy (anonymous):

I think A and C can be ruled out

OpenStudy (anonymous):

II and III only

OpenStudy (shadeyghost):

yup, that is what i believe too

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