New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

(2010) Kristen N. Stevens et al.   PLoS One

Molecular analysis ofPRKAG2,LAMP2, andNKX2-5genes in a cohort of 125 patients with accessory atrioventricular connection

(2009) Giorgia Esposito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Recurrence of Congenital Heart Defects in Families

(2009) Nina Øyen et al.   CIRCULATION

Familial transposition of the great arteries caused by multiple mutations in laterality genes

(2009) A. De Luca et al.   HEART

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

(2009) Erich Roessler et al.   MOLECULAR GENETICS AND METABOLISM

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

(2009) Steven C Greenway et al.   NATURE GENETICS

Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly

(2008) Erich Roessler et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

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