Beckwith-wiedemann syndrome, tumourigenesis and imprinting

This publication has 36 references indexed in Scilit:

• Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.
  Journal of Medical Genetics, 1992
• Monoallelic expression of the human H19 gene
  Nature Genetics, 1992
• Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
  Cell, 1991
• Chromosome 11 uniparental isodisomy predisposing to embryonal neoplasms
  The Lancet, 1991
• Familial predisposition to wilms tumor does not segregate with the WT1 gene
  Genomics, 1991
• Genomic imprinting
  The Lancet, 1991
• Dads and disomy and disease
  Nature, 1991
• Three‐generation dominant transmission of the Silver‐Russell syndrome
  American Journal of Medical Genetics, 1990
• Monozygotic twinning and structural defects
  The Journal of Pediatrics, 1979
• AUTOSOMAL-DOMINANT SEX-DEPENDENT TRANSMISSION OF THE WIEDEMANN-BECKWITH SYNDROME
  The Lancet, 1974