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1q32-q41 microdeletion with reference to van der Woude syndrome and allied clefting entities

✍ Scribed by Houdayer, Claude; Soupre, V�ronique; Karcenty, Bruno; Vazquez, Marie-Paule; Odent, Sylvie; Lacombe, Didier; Le Bouc, Yves; Munnich, Arnold; Bahuau, Michel

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
13 KB
Volume
91
Category
Article
ISSN
0148-7299

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Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
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## McIntosh Van der Woude syndrome (VWS) is an orofacial clefting disorder with an autosomal dominant pattern of inheritance. In our efforts to clone the VWS gene, 900 kb of genomic sequence from the VWS candidate region at chromosome 1q32-q41 was analyzed for new DNA sequence variants. We observed