Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

[1] Hoffman JI(2002)The incidence of congenital heart disease J Am Coll Cardiol 39 1890-1900

[2] Kaplan S(2004)Development gone awry: congenital heart disease Circ Res 94 273-283

[3] Gruber PJ(1983)Isolated ventricular septal defect in adults. Clinical and haemodynamic findings Br Heart J 50 343-348

[4] Epstein JA(2011)The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study Pediatr Cardiol 32 1147-1157

[5] Otterstad JE(2010)Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects J Pediatr 156 810-817

[6] Nitter-Hauge S(1999)Associations Between Chromosomal Anomalies and Congenital Heart Defects: A Database Search Am J Med Genet 84 158-166

[7] Myhre E(2007)Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients Eur Heart J 28 2778-2784

[8] Hartman RJ(2009)De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot Nat Genet 41 931-935

[9] Rasmussen SA(2008)High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease J Med Genet 45 704-709

[10] Botto LD(2012)Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease Am J Hum Genet 91 489-501

[1] Hoffman JI(2002)The incidence of congenital heart disease J Am Coll Cardiol 39 1890-1900

[2] Kaplan S(2004)Development gone awry: congenital heart disease Circ Res 94 273-283

[3] Gruber PJ(1983)Isolated ventricular septal defect in adults. Clinical and haemodynamic findings Br Heart J 50 343-348

[4] Epstein JA(2011)The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study Pediatr Cardiol 32 1147-1157

[5] Otterstad JE(2010)Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects J Pediatr 156 810-817

[6] Nitter-Hauge S(1999)Associations Between Chromosomal Anomalies and Congenital Heart Defects: A Database Search Am J Med Genet 84 158-166

[7] Myhre E(2007)Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients Eur Heart J 28 2778-2784

[8] Hartman RJ(2009)De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot Nat Genet 41 931-935

[9] Rasmussen SA(2008)High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease J Med Genet 45 704-709

[10] Botto LD(2012)Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease Am J Hum Genet 91 489-501