| Literature DB >> 10482882 |
Y Makita1, K Yamada, A Miyamoto, A Okuno, N Niikawa.
Abstract
We reported on a 5-year-old Japanese girl with clinical manifestations of Kabuki make-up syndrome (KMS) and van der Woude syndrome (VWS). Since the concurrence of the two syndromes is known in four patients, including ours, it suggests a common cause. Assuming that the association of the two syndromes was caused by a microdeletion involving the putative KMS/VWS genes, we carried out fluorescence in situ hybridization and microsatellite analyses using PAC clones and dinucleotide repeat markers spanning the VWS1 critical region at 1q32-q41. No deletion was detected at the VWS1 critical region. Copyright 1999 Wiley-Liss, Inc.Entities:
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Year: 1999 PMID: 10482882 DOI: 10.1002/(sici)1096-8628(19990917)86:3<285::aid-ajmg18>3.0.co;2-e
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299