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J Melki

Showing results (61-70 of 79) with videos related to

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Nature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
The Laryngoscope|July 20, 2010
Pharmacological protection of hearing loss in the mouse model of endolymphatic hydropsSami J Melki, Chris M Heddon, Jonathan K Frankel, et al.
Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
Journal of Cardiac Surgery|July 1, 1993
Intraoperative coronary angioscopy--technique and results: a study of 38 patientsJ P Bessou, J Melki, F Bouchart, et al.
Human Mutation|April 27, 2004
Allelic heterogeneity of SMARD1 at the IGHMBP2 locusI Maystadt, M Zarhrate, P Landrieu, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
American Journal of Human Genetics|July 1, 1993
Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genesC Boileau, G Jondeau, M C Babron, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Nature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1994
[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies]J Melki, S Lefebvre, L Burglen, et al.
The Laryngoscope|July 20, 2010
Pharmacological protection of hearing loss in the mouse model of endolymphatic hydropsSami J Melki, Chris M Heddon, Jonathan K Frankel, et al.
Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
Journal of Cardiac Surgery|July 1, 1993
Intraoperative coronary angioscopy--technique and results: a study of 38 patientsJ P Bessou, J Melki, F Bouchart, et al.
Human Mutation|April 27, 2004
Allelic heterogeneity of SMARD1 at the IGHMBP2 locusI Maystadt, M Zarhrate, P Landrieu, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
American Journal of Human Genetics|July 1, 1993
Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genesC Boileau, G Jondeau, M C Babron, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
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