Chromosome 22q11 monosomy and the genetic basis of congenital heart disease

This publication has 7 references indexed in Scilit:

• Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study
  The Journal of Pediatrics, 1996
• 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot
  Human Genetics, 1995
• Toward a Molecular Understanding of Congenital Heart Disease
  Circulation, 1995
• The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)
  New England Journal of Medicine, 1994
• Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
  Journal of Medical Genetics, 1993
• Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
  Nature Genetics, 1993
• Deletions within chromosome 22q11 in familial congenital heart disease
  The Lancet, 1992