Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Eitemau Tebyg

• Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
  gan: Cordell, H, et al.
  Cyhoeddwyd: (2013)
• Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
  gan: Cordell, H, et al.
  Cyhoeddwyd: (2013)
• Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
  gan: Soemedi, R, et al.
  Cyhoeddwyd: (2012)
• Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
  gan: Soemedi, R, et al.
  Cyhoeddwyd: (2012)
• Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
  gan: Soemedi, R, et al.
  Cyhoeddwyd: (2012)