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
โฆ LIBER โฆ
Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome
โ Scribed by Usha T. Sundaram; Donna M. McDonald-McGinn; Dale Huff; Beverly S. Emanuel; Elaine H. Zackai; Deborah A. Driscoll; Joann Bodurtha
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 73 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
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