Biology 2e
Biology 2e
2nd Edition
ISBN: 9781947172517
Author: Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher: OpenStax
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Chapter 13, Problem 11RQ

The genotype XXY corresponds to

  1. Klinefelter syndrome
  2. Turner syndrome
  3. Triplo-X
  4. Jacob syndrome

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AaBBdd x AaBbDd punnet square  genotype  phenotype
AaBbDd x AaBbDd   Punnet square  Phenotype Genotype
is thal ui ANensn hilia is an inherited genetic disorder linked to the nosome that results in ineffective blood clotting when a blood is damaged. The most common type, hemophilia A, occurs 5000 male births. Any male who carries the gene will express enotype. Hemophilia is extremely rare in women. Parents Carrler female Normal male couple wish to have children. The woman knows she a rrier for hemophilia. The man is not a hemophiliac. Use e notation Xh for hemophilia and XH for the dominant ele to complete the diagram on the right including the arent genotypes, gametes and possible fertilizations. rite the genotypes and phenotypes in the table below. XY XhXh Gametes Xh Xh Genotypes Phenotypes Possible lertilizations Male children XhY Xhx XhY XhX Paternal gametes Paternal gametes Female children 00 00 A second couple also wish to have children. The woman knows her maternal grandfather was a hemophiliac, but neither her mother or father were. Determine the probability she is a carrier…
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY