Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: A provisionally unique genetic syndrome?

✍ Scribed by Grosso, S. ;Farnetani, M.A. ;Berardi, R. ;Vivarelli, R. ;Vanni, M. ;Morgese, G. ;Balestri, P.

• Book ID: 101440929
• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 66 KB
• Volume: 111
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.10493