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Pediatric Research|February 18, 1999
Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 geneB Köhler, V Schumacher, U Schulte-Overberg, et al.
Pediatric Nephrology (Berlin, Germany)|October 1, 1989
Purine enzyme defects as a cause of acute renal failure in childhoodH A Simmonds, J S Cameron, T M Barratt, et al.
The British Journal of Dermatology|October 1, 1996
Fulminant metastatic calcinosis with cutaneous necrosis in a child with end-stage renal disease and tertiary hyperparathyroidismC C Zouboulis, U Blume-Peytavi, T Lennert, et al.
Nature Genetics|July 1, 1994
Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.
Human Genetics|November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelicB Wirth, K Zerres, M Fischbach, et al.
British Medical Journal|July 2, 1977
Prognosis of Henoch-Schönlein nephritis in childrenR Counahan, M H Winterborn, R H White, et al.
Archives of Disease in Childhood|May 1, 1985
Long term prognosis of recurrent haematuriaP F Miller, N I Speirs, S R Aparicio, et al.
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