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European Neurology|January 1, 1996

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.

Clinical Chemistry|July 1, 1996

Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12A Vandenberghe, P Latour, G Chauplannaz, et al.

Human Molecular Genetics|November 18, 1998

NF2 gene in neurofibromatosis type 2 patientsJ Zucman-Rossi, P Legoix, H Der Sarkissian, et al.

Human Genetics|August 1, 1996

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.

Neurogenetics|March 25, 2000

Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.

European Neurology|January 1, 1997

New mutations in the X-linked form of Charcot-Marie-Tooth diseaseP Latour, A Fabreguette, C Ressot, et al.

Revue Neurologique|January 29, 2005

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.

American Journal of Human Genetics|May 1, 1997

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.

Journal of Gynecology Obstetrics and Human Reproduction|April 14, 2017

Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospitalL Pons, M Till, E Alix, et al.

Revue Neurologique|August 20, 2013

[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.

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

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You have reached the last page of results.This site can display upto 20 results.

European Neurology|January 1, 1996

Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.

Clinical Chemistry|July 1, 1996

Human Molecular Genetics|November 18, 1998

NF2 gene in neurofibromatosis type 2 patientsJ Zucman-Rossi, P Legoix, H Der Sarkissian, et al.

Human Genetics|August 1, 1996

X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.

Neurogenetics|March 25, 2000

Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.

European Neurology|January 1, 1997

New mutations in the X-linked form of Charcot-Marie-Tooth diseaseP Latour, A Fabreguette, C Ressot, et al.

Revue Neurologique|January 29, 2005

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]R Ben Yaou, H-M Bécane, L Demay, et al.

American Journal of Human Genetics|May 1, 1997

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.

Journal of Gynecology Obstetrics and Human Reproduction|April 14, 2017

Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospitalL Pons, M Till, E Alix, et al.

Revue Neurologique|August 20, 2013

[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]V Humbertclaude, D Hamroun, M-C Picot, et al.

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