Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers

INTRODUCTION: Williams-Beuren syndrome (WBS; OMIM 194050) is caused by a hemizygous contiguous gene microdeletion at 7q11.23. Supravalvular aortic stenosis, mental retardation, overfriendliness, and ocular and renal abnormalities comprise typical symptoms in WBS. Although fluorescence in situ hybrid...

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Bibliographic Details
Main Authors: Dutra, Roberta Lelis, de Campos Pieri, Patrícia, Teixeira, Ana Carolina Dias, Honjo, Rachel Sayuri, Bertola, Debora Romeo, Kim, Chong Ae
Format: Artigo
Language:Inglês
Published: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2011
Subjects:
Clinical Science
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3129970/
https://ncbi.nlm.nih.gov/pubmed/21808859
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1807-59322011000600007
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