Hemophilia is a blood clotting disorder that is a sex-linked trait carried on the X chromosome. If a woman with hemophilia and a man without the disorder have two sons and two daughters, how many of their children would have hemophilia None One Two Four
Do a Punnett square. The first step is come up with names for your alleles. The woman has two X chromosomes and the man has one X and one Y chromosome. Because the woman has hemophilia and hemophilia is recessive, both her X chromosomes must have the hemophilia allele for her to have the disease. So you can label that particular allele Xh for X (the chromosome it is on) and h (the hemophilia allele). Her genotype is Xh Xh. The Dad does not have hemophilia, so he must have a normal X allele. His genotype is XY. These are the genotypes you should use in your Punnet square. Helpful?
What is a Punnett square, I fear I may have not learned that yet, or do not remember. Should I just google it?
Wikipedia would be better than Google. The Punnett Square for this cross looks like this: |dw:1351204642593:dw| The Mom's alleles are on the top, the Dad's alleles are on the side and the offspring's alleles will be in the squares.
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