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Head and neck manifestations of 22q11.2 deletion syndromes

✍ Scribed by Tal Marom; Yehudah Roth; Abraham Goldfarb; Udi Cinamon

Book ID: 106084537
Publisher: Springer-Verlag
Year: 2011
Tongue: English
Weight: 292 KB
Volume: 269
Category: Article
ISSN: 0302-9530
DOI: 10.1007/s00405-011-1745-1

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Letter to the Editor ## Opitz GBBB Syndrome and the 22q11.2 Deletion To the Editor: Recently, McDonald-McGinn et al. [1995] reported the presence of a deletion 22q11.2 in a family with autosomal dominant inheritance and in a sporadic case with the Opitz GBBB syndrome.The presence of a vascular r