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I am asked to fill the genotypes in the spaces provided but looks like I am aving a little bit of trouble. can anyone help? thanks in advance!

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Here are a few hints that might help:

Talking about Maria's pedigree: Firstly, it seems as if you have mixed up with $X^a$ and $X^A$, see that the disorder is X-linked DOMINANT. Anyone with either heterozygous or homozygous dominant expression would have the disease expressed. So the first generation male should have a genotype: $X^aY$, because if it were $X^AY$ then Amelogenesis imperfecta would be expressed as his phenotype and the first generation female should have a homozygous recessive genotype. Also no child in the second generation would suffer from the same. (NOTE: The one suffering from Amelogenesis in the second generation would have genotype $X^AY$)

As for Gunther disease, both the parent in the first generation should have a heterozygous dominant expression and the offspring suffering must have a homozygous recessive expression. And you can apply the same basics in Peter's pedigree.

I think this much should be enough to complete the task, but if you still have some doubt you can put it forward in the comments.

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Thank you very much Shefali for the explanation. I truly appreciate it. Here is my second attempt:… does it look ok now? Thanks in advance. Sorry for the inconvenience :) – ApothemCyte Jan 27 '14 at 3:34
Well, in the first place I did not understand what does H or h and - indicate? – Shefali Jan 27 '14 at 7:05
@ApothemCyte U have written Gg for peter's father but he could also be GG ! – biogirl Jan 27 '14 at 8:18
@Shefali Hello Shefali. Would you please if at all possible be able to help with my new question:… Thank you so much in advance!! – ApothemCyte Feb 19 '14 at 17:02

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