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Kidney International|June 16, 2006
A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disordersN Besbas, D Karpman, D Landau, et al.Journal of the American Society of Nephrology : JASN|December 16, 1998
Human complement factor H deficiency associated with hemolytic uremic syndromeN Rougier, M D Kazatchkine, J P Rougier, et al.American Journal of Human Genetics|October 1, 1994
Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel geneA F van Lieburg, M A Verdijk, V V Knoers, et al.American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.European Journal of Pediatrics|July 1, 1996
Verocytotoxin-producing Escherichia coli infection in hemolytic uremic syndrome in part of western EuropeN C van de Kar, H G Roelofs, H L Muytjens, et al.American Journal of Human Genetics|April 1, 1997
Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutationsL A Schimmenti, H E Cunliffe, L A McNoe, et al.American Journal of Human Genetics|February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndromeJ Kohlhase, P E Taschner, P Burfeind, et al.Pageof 13