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M L Mostacciuolo

Showing results (11-20 of 58) with videos related to

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Genetic Epidemiology|January 1, 1987
Genetic epidemiology of myotonic dystrophyM L Mostacciuolo, G Barbujani, M Armani, et al.
Human Genetics|March 1, 1987
Population data on benign and severe forms of X-linked muscular dystrophyM L Mostacciuolo, A Lombardi, V Cambissa, et al.
American Journal of Medical Genetics|November 7, 1998
Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysisF A Saad, L Merlini, M L Mostacciuolo, et al.
Neuroepidemiology|January 1, 1992
Epidemiology of spinal muscular atrophies in a sample of the Italian populationM L Mostacciuolo, G A Danieli, C Trevisan, et al.
Human Genetics|January 1, 1980
Duchenne muscular dystrophy: data from family studiesG A Danieli, M L Mostacciuolo, G Pilotto, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entityM L Mostacciuolo, L Rampoldi, E Righetti, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
PCR Methods and Applications|August 1, 1993
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP)F A Saad, L Vitiello, S Oliviero, et al.
American Journal of Human Genetics|July 6, 2000
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28G Vazza, M Zortea, F Boaretto, et al.
Human Genetics|May 1, 1993
Patterns of deletions of the dystrophin gene in different European populationsG A Danieli, F Mioni, C R Müller, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Genetic Epidemiology|January 1, 1987
Genetic epidemiology of myotonic dystrophyM L Mostacciuolo, G Barbujani, M Armani, et al.
Human Genetics|March 1, 1987
Population data on benign and severe forms of X-linked muscular dystrophyM L Mostacciuolo, A Lombardi, V Cambissa, et al.
American Journal of Medical Genetics|November 7, 1998
Double missense mutation in exon 41 of the human dystrophin gene detected by double strand conformation analysisF A Saad, L Merlini, M L Mostacciuolo, et al.
Neuroepidemiology|January 1, 1992
Epidemiology of spinal muscular atrophies in a sample of the Italian populationM L Mostacciuolo, G A Danieli, C Trevisan, et al.
Human Genetics|January 1, 1980
Duchenne muscular dystrophy: data from family studiesG A Danieli, M L Mostacciuolo, G Pilotto, et al.
Neuromuscular Disorders : NMD|September 21, 2000
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entityM L Mostacciuolo, L Rampoldi, E Righetti, et al.
Neuroepidemiology|January 1, 1995
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1M L Mostacciuolo, F Schiavon, C Angelini, et al.
PCR Methods and Applications|August 1, 1993
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP)F A Saad, L Vitiello, S Oliviero, et al.
American Journal of Human Genetics|July 6, 2000
A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28G Vazza, M Zortea, F Boaretto, et al.
Human Genetics|May 1, 1993
Patterns of deletions of the dystrophin gene in different European populationsG A Danieli, F Mioni, C R Müller, et al.
Pageof 6