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M L Mostacciuolo

Showing results (31-40 of 58) with videos related to

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Journal of Medical Genetics|June 19, 2002
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1M Zortea, A Vettori, C P Trevisan, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Human Genetics|July 1, 1987
Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibshipsA Russo, G Barbujani, M L Mostacciuolo, et al.
Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.
Neurology|August 27, 2003
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutationF Dalpozzo, M G Rossetto, F Boaretto, et al.
Advances in Experimental Medicine and Biology|January 1, 1987
Familial ALS: clinical, genetic and morphological featuresM Armani, S Pierobon-Bormioli, M L Mostacciuolo, et al.
Human Genetics|May 1, 1991
X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric regionM L Mostacciuolo, E Müller, P Fardin, et al.
American Journal of Human Genetics|December 11, 2002
A locus for migraine without aura maps on chromosome 14q21.2-q22.3D Soragna, A Vettori, G Carraro, et al.
Human Molecular Genetics|January 1, 1994
Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)N Fairweather, C Bell, S Cochrane, et al.
Human Mutation|January 1, 1997
Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysisF A Saad, M L Mostacciuolo, C P Trevisan, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Journal of Medical Genetics|June 19, 2002
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1M Zortea, A Vettori, C P Trevisan, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Human Genetics|July 1, 1987
Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibshipsA Russo, G Barbujani, M L Mostacciuolo, et al.
Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.
Neurology|August 27, 2003
Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutationF Dalpozzo, M G Rossetto, F Boaretto, et al.
Advances in Experimental Medicine and Biology|January 1, 1987
Familial ALS: clinical, genetic and morphological featuresM Armani, S Pierobon-Bormioli, M L Mostacciuolo, et al.
Human Genetics|May 1, 1991
X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric regionM L Mostacciuolo, E Müller, P Fardin, et al.
American Journal of Human Genetics|December 11, 2002
A locus for migraine without aura maps on chromosome 14q21.2-q22.3D Soragna, A Vettori, G Carraro, et al.
Human Molecular Genetics|January 1, 1994
Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)N Fairweather, C Bell, S Cochrane, et al.
Human Mutation|January 1, 1997
Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysisF A Saad, M L Mostacciuolo, C P Trevisan, et al.
Pageof 6