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A missense mutation in the ZFHX1B gene associated with an atypical Mowat–Wilson syndrome phenotype

✍ Scribed by Wolfram Heinritz; Christiane Zweier; Ursula G. Froster; Sibylle Strenge; Annegret Kujat; Steffen Syrbe; Anita Rauch; Volker Schuster

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 214 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31267

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