Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome
โ Scribed by Hiroyuki Yamagishi; Deepak Srivastava
- Book ID
- 117788093
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 849 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1471-4914
No coin nor oath required. For personal study only.
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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