Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1
- 1 April 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (4) , 1420-1425
- https://doi.org/10.1086/302864
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Signaling from Rho to the Actin Cytoskeleton Through Protein Kinases ROCK and LIM-kinaseScience, 1999
- Rearrangement of the HumanCDC5LGene by a t(6;19)(p21;q13.1) in a Patient with Multicystic Renal DysplasiaGenomics, 1998
- Systemic autoimmune nephritogenic components induce CSF-1 and TNF-α in MRL kidneysKidney International, 1997
- Genetic dissection of complex traits: guidelines for interpreting and reporting linkage resultsNature Genetics, 1995
- Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral refluxNature Genetics, 1995
- Evidence for genetic heterogeneity in hereditary hydronephrosis caused by pelvi-ureteric junction obstruction, with one locus assigned to chromosome 6pHuman Genetics, 1992
- HLA linkage with familial vesicoureteral reflux and familial pelvi‐ureteric junction obstructionTissue Antigens, 1989
- A ras-related gene with transformation suppressor activityCell, 1989
- A novel ras-related gene familyCell, 1985
- A family study of vesicoureteric refluxJournal of Medical Genetics, 1978