R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease

Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

(2010) B Stallmeyer et al.   CLINICAL GENETICS

NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD)

(2010) Stella Marie Reamon-Buettner et al.   HUMAN MUTATION

Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project

(2009) Sallie B Freeman et al.   GENETICS IN MEDICINE

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot

(2009) R. Rauch et al.   JOURNAL OF MEDICAL GENETICS

Examining the Cardiac NK-2 Genes in Early Heart Development

(2009) Heather Bartlett et al.   PEDIATRIC CARDIOLOGY

NKX2.5 mutations in patients with non-syndromic congenital heart disease

(2008) Luciana Gioli-Pereira et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY