COL11A2 mutation associated with autosomal recessive Weissenbacher–Zweymuller syndrome: Molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED)

✍ Scribed by Tamar Harel; Ronen Rabinowitz; Netta Hendler; Aharon Galil; Hagit Flusser; Juan Chemke; Libe Gradstein; Tova Lifshitz; Rivka Ofir; Khalil Elbedour; Ohad S. Birk

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 60 KB
• Volume: 132A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.30371