Estimating prevalence in single-gene kidney diseases progressing to renal failure
- 1 September 2000
- journal article
- review article
- Published by Elsevier BV in Kidney International
- Vol. 58 (3), 925-943
- https://doi.org/10.1046/j.1523-1755.2000.00250.x
Abstract
No abstract availableKeywords
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 cMAmerican Journal of Human Genetics, 1999
- Prevalence of tuberous sclerosis estimated by capture-recapture analysisThe Lancet, 1998
- Molecular genetic identification of families with juvenile nephronophthisis type 1: Rate of progression to renal failureKidney International, 1997
- Case Counting in Epidemiology: Limitations of Methods Based on Multiple Data SourcesInternational Journal of Epidemiology, 1996
- Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13Annals of Human Genetics, 1994
- Primary hyperoxaluria type IEuropean Journal of Pediatrics, 1990
- High incidence of Bardet Biedl syndrome among the BedouinClinical Genetics, 1989
- The Cardinal Manifestations of Bardet–Biedl Syndrome, a Form of Laurence–Moon–Biedl SyndromeNew 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