Ventricular septal defect associated with microdeletions of chromosome 22q11.2
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.580612.x/fullpdf
Reference25 articles.
1. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11;Driscoll;Am J Hum Genet,1992
2. The velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus;Scambler;Lancet,1992
3. Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11;Burn;J Med Genet,1993
4. CATCH22 [editorial];Hall;J Med Genet,1993
5. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet,1997
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