Genetic players in esophageal atresia and tracheoesophageal fistula

This publication has 46 references indexed in Scilit:

• MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome
  Nature Genetics, 2005
• Association of anophthalmia and esophageal atresia: Four new cases identified by the anophthalmia/microphthalmia clinical registry
  American Journal of Medical Genetics Part A, 2004
• Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
  Nature Genetics, 2004
• Hedgehog and PI-3 kinase signaling converge on Nmyc1 to promote cell cycle progression in cerebellar neuronal precursors
  Development, 2004
• Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?
  Trends in Genetics, 2003
• Feingold syndrome: Clinical review and genetic mapping
  American Journal of Medical Genetics Part A, 2003
• Interstitial deletion of chromosome 17 (del(17)(q22q23.3)) confirms a link with oesophageal atresia
  Journal of Medical Genetics, 2000
• The effects of Down syndrome and other chromosomal abnormalities on survival and management in oesophageal atresia
  Pediatric Surgery International, 1997
• Additional congenital anomalies in babies with gut atresia or stenosis: when to investigate, and which investigation
  Pediatric Surgery International, 1997
• Familial occurrence of congenital laryngeal clefts
  Archives of Disease in Childhood, 1973