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Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1

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Presentation on theme: "Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1"— Presentation transcript:

1 Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1
Andrew R. Zinn, Vijay S. Tonk, Zhong Chen, Wendy L. Flejter, H. Allen Gardner, Rudy Guerra, Harvey Kushner, Stuart Schwartz, Virginia P. Sybert, Daniel L. Van Dyke, Judith L. Ross  The American Journal of Human Genetics  Volume 63, Issue 6, Pages (December 1998) DOI: /302152 Copyright © 1998 The American Society of Human Genetics Terms and Conditions

2 Figure 1 Graphic representation of deletions. Bars represent material present in deleted X chromosomes. Positions of molecular-cytogenetic markers are indicated. The American Journal of Human Genetics  , DOI: ( /302152) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

3 Figure 2 Strength of associations between deleted markers and five phenotypic traits: adjusted height, ovarian failure (ovary), high-arched palate (palate), thyroid autoantibodies (thyroid), and increased carrying angle of the elbow (carrying angle). A score of “0” indicates that there is no association. Scores >∼3 are statistically significant (see Subjects and Methods). The American Journal of Human Genetics  , DOI: ( /302152) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

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