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Author6 Posts
  #1

a man is affected with tyrosinase-negative oculocutaneous albinism (autosomal recessive). Based on this information alone, what is the probability that his grandson and his great-granddaughter are both heterozygous carriers of the albinism gene?

can anyone ans this with an explanation?

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I hear and I forget. I see and I remember. I do and I understand.
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  #2

I don't think its possible to calculate as there isn't ample information.

  #3

Since he has it (aa), his child that delivered his grandson must be a carrier (at least). So his grandson should have 1/2 probability and his greatgranddaugther should have 1/4 probablity as a carrier.

  #4

well according to this site, the answer is 1/8 and they didnt give any explanation:

http://medgen.genetics.utah.edu/tests/test11995/q...

  #5

Because they are asking the probality of both happening
1/2 *1/4 =1/8

  #6

here is my explanation :

1.all of his children will be carriers
2.50% of his grandchildren willl be heterozygus NO matter the female mate genotype (= if she is carrier, homozygus for recessive or dominant genes)
3.the same situation also for next generation

calculating --> 1/8

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