Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients

This publication has 40 references indexed in Scilit:

• Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping
  Human Molecular Genetics, 1993
• Pigmented Fundus Lesions in a Preterm Infant With Familial Adenomatous Polyposis
  Archives of Ophthalmology (1950), 1993
• Fundus Changes Associated With Congenital Hypertrophy of the Retinal Pigment Epithelium
  American Journal of Ophthalmology, 1993
• Familial adenomatous polyposis (Gardner's syndrome) and thyroid carcinoma
  Digestive Diseases and Sciences, 1993
• The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.
  Journal of Medical Genetics, 1991
• Importance of retinal pigmentation as a subclinical marker in familial adenomatous polyposis
  Diseases of the Colon & Rectum, 1990
• Common Inheritance of Susceptibility to Colonic Adenomatous Polyps and Associated Colorectal Cancers
  New England Journal of Medicine, 1988
• Localization of the gene for familial adenomatous polyposis on chromosome 5
  Nature, 1987
• The Incidence and Prevalence of Familial Polyposis Coli in Denmark
  Scandinavian Journal of Social Medicine, 1986
• Hypertrophy of the Retinal Pigment Epithelium Associated with Gardner's Syndrome
  American Journal of Ophthalmology, 1980