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The Turner Syndrome–Associated Neurocognitive Phenotype Maps to Distal Xp
Judith L. Ross, David Roeltgen, Harvey Kushner, Fanglin Wei, Andrew R. Zinn The American Journal of Human Genetics Volume 67, Issue 3, Pages (September 2000) DOI: /303039 Copyright © 2000 The American Society of Human Genetics Terms and Conditions
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Figure 1 Mapping of subjects with nonmosaic Xp deletions. Related subjects are indicated. Bars indicate regions present. Shaded bars indicate subjects with TS neurocognitive phenotype. Approximate physical distances are shown on the left. Deletions are grouped according to results of FISH, with markers shown on the right; order of subjects within groups is arbitrary. The American Journal of Human Genetics , DOI: ( /303039) Copyright © 2000 The American Society of Human Genetics Terms and Conditions
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Figure 2 The neurocognitive phenotype maps to distal Xp. Data for deletion mapping, X inactivation, parent of origin (p = paternal, m = maternal), and neurocognitive phenotype are shown for the eight subjects with the smallest terminal deletions and for two subjects with interstitial deletions (fig. 1). Black lines indicate regions not deleted; gray lines indicate uncertainty. Underscored subjects indicate mother-daughter pairs; double-underscored subjects indicate mz twins. The American Journal of Human Genetics , DOI: ( /303039) Copyright © 2000 The American Society of Human Genetics Terms and Conditions
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