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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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M Fischbach

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Molecular Syndromology|December 23, 2011

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.

Nephrologie & Therapeutique|July 16, 2013

[Focusing on peritoneal dialysis adequacy]Belkacem Issad, Pierre-Yves Durand, Pascale Siohan, et al.

Clinical and Experimental Rheumatology|August 21, 2001

The French version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)J Pouchot, N Ruperto, I Lemelle, et al.

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Search research articles

Showing results (171-180 of 173) with videos related to

Sort By:

Pageof 18

You have reached the last page of results.This site can display upto 173 results.

Molecular Syndromology|December 23, 2011

Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyE Schaefer, A Zaloszyc, J Lauer, et al.

Nephrologie & Therapeutique|July 16, 2013

[Focusing on peritoneal dialysis adequacy]Belkacem Issad, Pierre-Yves Durand, Pascale Siohan, et al.

Clinical and Experimental Rheumatology|August 21, 2001

The French version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)J Pouchot, N Ruperto, I Lemelle, et al.

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