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Steven J Scheinman

Showing results (21-30 of 25) with videos related to

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Nephron. Physiology|April 25, 2009
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variabilityAntony E Shrimpton, Richard R Hoopes, Stephen J Knohl, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 5, 2016
Glomerular Pathology in Dent Disease and Its Association with Kidney FunctionXiangling Wang, Franca Anglani, Lada Beara-Lasic, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 11, 2014
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, et al.
Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Nephron. Physiology|April 25, 2009
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variabilityAntony E Shrimpton, Richard R Hoopes, Stephen J Knohl, et al.
Clinical Journal of the American Society of Nephrology : CJASN|October 5, 2016
Glomerular Pathology in Dent Disease and Its Association with Kidney FunctionXiangling Wang, Franca Anglani, Lada Beara-Lasic, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 11, 2014
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, et al.
Nature Genetics|February 12, 2013
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencingAndrew Kirby, Andreas Gnirke, David B Jaffe, et al.
Nephron. Physiology|February 26, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsGraciana Jaureguiberry, Muriel De la Dure-Molla, David Parry, et al.
Pageof 3