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A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence ofTBX5 mutations: Report of a Thai family

✍ Scribed by Kantaputra, Piranit N. ;Yamasaki, Kentaro ;Ishida, Takafumi ;Kishino, Tatsuya ;Niikawa, Norio


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
279 KB
Volume
111
Category
Article
ISSN
0148-7299

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Van der Woude syndrome with sensorineura
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## Abstract A four‐generation Thai family affected with Van der Woude syndrome is reported. The disorder appeared to be originally inherited from a person who was half Thai and half Pakistani. The lip lesions found in this family were varied and did not appear to be related to other phenotypes. The