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Lancet (London, England)|November 14, 2001
Autosomal dominant polycystic kidney disease: modification of disease progressionD J Peters, M H BreuningTrends in Genetics : TIG|June 5, 1998
Conjunction dysfunction: CBP/p300 in human diseaseR H Giles, D J Peters, M H BreuningNephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of translation terminating mutations in the PKD1 geneJ H Roelfsema, D J Peters, M H BreuningEuropean Journal of Human Genetics : EJHG|February 13, 2002
Mutation detection for exons 2 to 10 of the polycystic kidney disease 1 (PKD1)-gene by DGGED J Peters, Y Ariyurek, M van Dijk, et al.Journal of the American Society of Nephrology : JASN|September 7, 1999
The angiotensin-converting enzyme genotype and microalbuminuria in autosomal dominant polycystic kidney diseaseM A van Dijk, D J Peters, M H Breuning, et al.European Journal of Human Genetics : EJHG|December 22, 1999
Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2)B Veldhuisen, L Spruit, H G Dauwerse, et al.Journal of the American Society of Nephrology : JASN|December 1, 1995
Intracranial aneurysms in polycystic kidney disease linked to chromosome 4M A van Dijk, P C Chang, D J Peters, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 1, 2000
The ACE insertion/deletion polymorphism has no influence on progression of renal function loss in autosomal dominant polycystic kidney diseaseM A van Dijk, M H Breuning, D J Peters, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Analysis of a large family with the second type of autosomal dominant polycystic kidney diseaseB Veldhuisen, M H Breuning, E Wesby-van Swaay, et al.Nederlands Tijdschrift Voor Geneeskunde|November 14, 2002
[Phenotypic variability: genetics and chance--deletion 22q11 and schizophrenia]M H BreuningPageof 24