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Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome

✍ Scribed by Schutte, Brian C.; Basart, Ann M.; Watanabe, Yoriko; Laffin, Jennifer J.S.; Coppage, Kevin; Bjork, Bryan C.; Daack-Hirsch, Sandy; Patil, Shiva; Dixon, Michael J.; Murray, Jeffrey C.

Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
27 KB
Volume
84
Category
Article
ISSN
0148-7299

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✦ Synopsis

Van der Woude syndrome (VWS) is an autosomal dominant disorder comprising cleft lip and/or cleft palate and lip pits. We reported previously a family whose underlying mutation is a 500-800 kb deletion localized to chromosome bands 1q32-q41 [Sander et al.,

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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