Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease
- 1 November 1992
- journal article
- Published by Elsevier in The Lancet
- Vol. 340 (8831) , 1330-1333
- https://doi.org/10.1016/0140-6736(92)92503-8
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneityClinical Genetics, 2008
- Counselling under genetic heterogeneity: a practical approachClinical Genetics, 2008
- Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite markerThe Lancet, 1991
- Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).Journal of Medical Genetics, 1990
- Autosomal dominant Polycystic Kidney Disease: A linkage evaluation of heterogeneity in ItalyAmerican Journal of Medical Genetics, 1990
- Linkage Heterogeneity of Autosomal Dominant Polycystic Kidney DiseaseNew England Journal of Medicine, 1988
- A SECOND GENETIC LOCUS FOR AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASEThe Lancet, 1988
- A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16Nature, 1985
- Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: Data for genetic counsellingAmerican Journal of Medical Genetics, 1984
- Nonparametric Estimation from Incomplete ObservationsJournal of the American Statistical Association, 1958