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G Deschenes

Showing results (11-20 of 15) with videos related to

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American Journal of Human Genetics|July 1, 1992
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragmentsB Knebelmann, G Deschenes, F Gros, et al.
Human Genetics|December 1, 1992
Alport syndrome: a genetic study of 31 familiesR M'Rad, M Sanak, G Deschenes, 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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31M Vollmer, N Jeck, H H Lemmink, et al.
The Journal of Clinical Endocrinology and Metabolism|July 28, 2015
CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive TraitA Molin, R Baudoin, M Kaufmann, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
American Journal of Human Genetics|July 1, 1992
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragmentsB Knebelmann, G Deschenes, F Gros, et al.
Human Genetics|December 1, 1992
Alport syndrome: a genetic study of 31 familiesR M'Rad, M Sanak, G Deschenes, 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.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2000
Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31M Vollmer, N Jeck, H H Lemmink, et al.
The Journal of Clinical Endocrinology and Metabolism|July 28, 2015
CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive TraitA Molin, R Baudoin, M Kaufmann, et al.
Pageof 2