Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00290.x/fullpdf
Reference55 articles.
1. Cardiac anomalies associated with a chromosome 22q11.2 deletion in patients with conotruncal anomaly face syndrome;Momma;Am J Cardiol,1996
2. Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study;Ryan;J Med Genet,1997
3. 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin;Fokstuen;Clin Genet,1998
4. Prevalence and parental origin in tetralogy of Fallot associated with chromosome 22q11 microdeletion;Lu;Pediatrics,1999
5. Anatomic patterns of conotruncal defects associated with deletion 22q11;Marino;Genet Med,2001
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