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Can I read Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome on EtoBox?

Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome 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. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

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

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.,

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

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
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; Wiley (John Wiley & Sons); Wiley-Liss Inc; Wiley (ISSN 0148-7299)
Published
1999
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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Browse all works 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.