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Pascal Reynier

Showing results (241-250 of 245) with videos related to

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Diagnostics (Basel, Switzerland)|February 13, 2026
Systemic Inflammatory and Hematological Profiles in Triple-Negative Breast Cancer: A Study from a Senegalese CohortNènè Oumou Kesso Barry, Mamadou Sow, Pape Matar Kandji, et al.
Journal of Medical Genetics|July 13, 2013
Prevalence of rare mitochondrial DNA mutations in mitochondrial disordersSylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre, et al.
JAMA Neurology|November 29, 2017
Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young AdultsMajida Charif, Alessia Nasca, Kyle Thompson, et al.
Human Molecular Genetics|April 12, 2015
A common variant near TGFBR3 is associated with primary open angle glaucomaZheng Li, R Rand Allingham, Masakazu Nakano, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 25

Showing results (241-250 of 245) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 245 results.
Diagnostics (Basel, Switzerland)|February 13, 2026
Systemic Inflammatory and Hematological Profiles in Triple-Negative Breast Cancer: A Study from a Senegalese CohortNènè Oumou Kesso Barry, Mamadou Sow, Pape Matar Kandji, et al.
Journal of Medical Genetics|July 13, 2013
Prevalence of rare mitochondrial DNA mutations in mitochondrial disordersSylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre, et al.
JAMA Neurology|November 29, 2017
Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young AdultsMajida Charif, Alessia Nasca, Kyle Thompson, et al.
Human Molecular Genetics|April 12, 2015
A common variant near TGFBR3 is associated with primary open angle glaucomaZheng Li, R Rand Allingham, Masakazu Nakano, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 25