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J Melki

Showing results (71-80 of 79) with videos related to

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Human Genetics|May 31, 2001
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMAL A Skordis, M G Dunckley, L Burglen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
Human Molecular Genetics|September 1, 1994
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2pJ Hazan, B Fontaine, R P Bruyn, et al.
Genomics|May 1, 1994
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophyC Mérette, L M Brzustowicz, R J Daniels, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 1, 2005
Mutation and methylation analysis of TP53 in adrenal carcinogenesisS Sidhu, E Martin, C Gicquel, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Neurology|October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosumC Goizet, A Boukhris, D Maltete, et al.
Clinical Genetics|September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disordersS Naudion, S Moutton, I Coupry, et al.
Neurology|March 27, 2009
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALSA-M Wills, S Cronin, A Slowik, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
Human Genetics|May 31, 2001
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMAL A Skordis, M G Dunckley, L Burglen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
Human Molecular Genetics|September 1, 1994
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2pJ Hazan, B Fontaine, R P Bruyn, et al.
Genomics|May 1, 1994
An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophyC Mérette, L M Brzustowicz, R J Daniels, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 1, 2005
Mutation and methylation analysis of TP53 in adrenal carcinogenesisS Sidhu, E Martin, C Gicquel, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Neurology|October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosumC Goizet, A Boukhris, D Maltete, et al.
Clinical Genetics|September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disordersS Naudion, S Moutton, I Coupry, et al.
Neurology|March 27, 2009
A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALSA-M Wills, S Cronin, A Slowik, et al.
Pageof 8