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C Rinat

Showing results (1-10 of 4) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 27, 2001
Familial inheritance of crossed fused renal ectopiaC Rinat, A Farkas, Y Frishberg
The Journal of Pediatrics|February 5, 2000
Hypothyroidism in primary hyperoxaluria type 1Y Frishberg, S Feinstein, C Rinat, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic groupC Rinat, R J Wanders, A Drukker, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 18, 2006
Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodiesR Becker-Cohen, M Bruschi, C Rinat, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Pediatric Nephrology (Berlin, Germany)|April 27, 2001
Familial inheritance of crossed fused renal ectopiaC Rinat, A Farkas, Y Frishberg
The Journal of Pediatrics|February 5, 2000
Hypothyroidism in primary hyperoxaluria type 1Y Frishberg, S Feinstein, C Rinat, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Primary hyperoxaluria type I: a model for multiple mutations in a monogenic disease within a distinct ethnic groupC Rinat, R J Wanders, A Drukker, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 18, 2006
Recurrent nephrotic syndrome in homozygous truncating NPHS2 mutation is not due to anti-podocin antibodiesR Becker-Cohen, M Bruschi, C Rinat, et al.
Pageof 1