Estimating prevalence in single-gene kidney diseases progressing to renal failure

This publication has 69 references indexed in Scilit:

• A Founder Effect in the Newfoundland Population Reduces the Bardet-Biedl Syndrome I (BBS1) Interval to 1 cM
  American Journal of Human Genetics, 1999
• Prevalence of tuberous sclerosis estimated by capture-recapture analysis
  Published by Elsevier ,1998
• Molecular genetic identification of families with juvenile nephronophthisis type 1: Rate of progression to renal failure
  Kidney International, 1997
• Case Counting in Epidemiology: Limitations of Methods Based on Multiple Data Sources
  International Journal of Epidemiology, 1996
• Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13
  Annals of Human Genetics, 1994
• Primary hyperoxaluria type I
  European Journal of Pediatrics, 1990
• High incidence of Bardet Biedl syndrome among the Bedouin
  Clinical Genetics, 1989
• The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl Syndrome
  New England Journal of Medicine, 1989
• Genetic aspects of tuberous sclerosis in the west of Scotland.
  Journal of Medical Genetics, 1989
• Congenital nephrotic syndrome of Finnish type. Study of 75 patients.
  Archives of Disease in Childhood, 1976