A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: Is this a candidate region for the syndrome?

✍ Scribed by J. Xu; Y.S. Fan; V.M. Siu

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 123 KB
• Volume: 146A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.32359