22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference68 articles.
1. Autosomal dominant “Opitz” GBBB syndrome due to a 22q11. 2 deletion
2. Seven new cases of cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case
3. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
4. DiGeorge syndrome: part of CATCH 22.
5. Closing time for CATCH22
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