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Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene

✍ Scribed by B. Gentilin; F. Forzano; M. F. Bedeschi; T. Rizzuti; F. Faravelli; C. Izzi; M. Lituania; C. Rodriguez-Perez; M. P. Bondioni; G. Savoldi; E. Grosso; G. Botta; E. Viora; A. M. Baffico; F. Lalatta

Book ID: 112229760
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 269 KB
Volume: 36
Category: Article
ISSN: 0960-7692
DOI: 10.1002/uog.7761

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