Molecular genetic analysis of familial neuroblastoma

This publication has 24 references indexed in Scilit:

• Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
  Nature Genetics, 1996
• A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease
  Cell, 1994
• Deletion of chromosome 11 and of 14q sequences in neuroblastoma
  Genes, Chromosomes and Cancer, 1993
• Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
  Nature Genetics, 1993
• Ondine-Hirschsprung syndrome (Haddad syndrome)
  European Journal of Pediatrics, 1993
• Constitutional translocation t(1;17)(p36;q12–21) in a patient with neuroblastoma
  Genes, Chromosomes and Cancer, 1990
• Familial Occurrence of Neuroblastoma, Von Recklinghausen's Neurofibromatosis, Hirschsprung's Agangliosis and Jaw‐winking Syndrome
  Acta Paediatrica, 1989
• Multifocal ganglioneuroblastoma coexistent with total colonic aganglionosis
  Journal of Pediatric Surgery, 1988
• Neurofibromatosis and Associated Neuroectodermal Tumors: A Congenital Neurocristopathy
  Pediatric Pathology, 1986
• Mutation and Cancer: Statistical Study of Retinoblastoma
  Proceedings of the National Academy of Sciences, 1971