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J Melki

Showing results (11-20 of 79) with videos related to

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American Journal of Human Genetics|May 1, 1992
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5qB Müller, J Melki, P Burlet, et al.
American Journal of Human Genetics|April 17, 1999
The promoters of the survival motor neuron gene (SMN) and its copy (SMNc) share common regulatory elementsA Echaniz-Laguna, P Miniou, D Bartholdi, et al.
Neuroreport|October 3, 1994
Early detection of mouse wobbler mutation: a model of pathological motoneurone deathV des Portes, M Coulpier, J Melki, et al.
American Journal of Medical Genetics|September 1, 1992
Parental origin of the X chromosomes in Rett syndromeL Benedetti, A Munnich, J Melki, et al.
Human Molecular Genetics|September 15, 1998
The role of the SMN gene in proximal spinal muscular atrophyS Lefebvre, L Bürglen, J Frézal, et al.
Revue Des Maladies Respiratoires|April 23, 2014
[Pulmonary resection using video-assisted thoracoscopic surgery--20 years experience]J-M Baste, B Orsini, P Rinieri, et al.
Journal De Chirurgie|February 1, 1990
[Late dehiscence of manual anastomosis of the small intestine]J Melki, B Bokobza, I Le Blanc, et al.
Neurochemistry International|May 28, 2010
Generalized molecular defects of the neuromuscular junction in skeletal muscle of the wobbler mutant mouseJ Melki, B Blondet, M Pinçon-Raymond, et al.
American Journal of Medical Genetics|January 1, 1990
Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome XH Journel, J Melki, C Turleau, et al.
Journal of Medical Genetics|January 1, 1997
De novo deletions in spinal muscular atrophy: implications for genetic counsellingV Raclin, P S Veber, L Bürglen, et al.
Pageof 8

Showing results (11-20 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|May 1, 1992
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5qB Müller, J Melki, P Burlet, et al.
American Journal of Human Genetics|April 17, 1999
The promoters of the survival motor neuron gene (SMN) and its copy (SMNc) share common regulatory elementsA Echaniz-Laguna, P Miniou, D Bartholdi, et al.
Neuroreport|October 3, 1994
Early detection of mouse wobbler mutation: a model of pathological motoneurone deathV des Portes, M Coulpier, J Melki, et al.
American Journal of Medical Genetics|September 1, 1992
Parental origin of the X chromosomes in Rett syndromeL Benedetti, A Munnich, J Melki, et al.
Human Molecular Genetics|September 15, 1998
The role of the SMN gene in proximal spinal muscular atrophyS Lefebvre, L Bürglen, J Frézal, et al.
Revue Des Maladies Respiratoires|April 23, 2014
[Pulmonary resection using video-assisted thoracoscopic surgery--20 years experience]J-M Baste, B Orsini, P Rinieri, et al.
Journal De Chirurgie|February 1, 1990
[Late dehiscence of manual anastomosis of the small intestine]J Melki, B Bokobza, I Le Blanc, et al.
Neurochemistry International|May 28, 2010
Generalized molecular defects of the neuromuscular junction in skeletal muscle of the wobbler mutant mouseJ Melki, B Blondet, M Pinçon-Raymond, et al.
American Journal of Medical Genetics|January 1, 1990
Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome XH Journel, J Melki, C Turleau, et al.
Journal of Medical Genetics|January 1, 1997
De novo deletions in spinal muscular atrophy: implications for genetic counsellingV Raclin, P S Veber, L Bürglen, et al.
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