Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2
β Scribed by M. Cristina Digilio; Donna M. McDonald-McGinn; Carrie Heike; Charles Catania; Bruno Dallapiccola; Bruno Marino; Elaine H. Zackai
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 103 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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The clinical manifestations of patients with a 22q11.2 deletion are highly variable and mainly include developmental defects of structures derived from the third and fourth pharyngeal pouches. Laryngeal atresia has occasionally been reported in Di-George syndrome as well as in velo-cardiofacial synd
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