Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M L Mostacciuolo

Showing results (1-10 of 58) with videos related to

Pageof 6
Sort By:
Minerva Pediatrica|August 31, 1986
[Steinert's dystrophia myotonica . Epidemiological and clinical aspects]M L Mostacciuolo, M Armani
Human Mutation|January 1, 1996
Novel missense mutation of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathyF Schiavon, C Fracasso, M L Mostacciuolo
Gene|October 7, 2003
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28G Vazza, S Picelli, A Bozzato, et al.
American Journal of Medical Genetics|March 1, 1989
Problems in genetic counseling in a family with an "atypical" centronuclear myopathyB Müller, M L Mostacciuolo, G A Danieli, et al.
Human Mutation|February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypesF Schiavon, A Rampazzo, L Merlini, et al.
Minerva Pediatrica|August 31, 1986
[Genetic counseling in hereditary neuromuscular diseases]G A Danieli, M L Mostacciuolo, P Marchesini, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
American Journal of Medical Genetics|June 15, 1991
Genetic epidemiology of hereditary motor sensory neuropathies (type I)M L Mostacciuolo, G Micaglio, P Fardin, et al.
Neuromuscular Disorders : NMD|October 21, 2006
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onsetG Vazza, L Merlini, C Bertolin, et al.
Human Genetics|November 1, 1992
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia)E Müller, M L Mostacciuolo, G Micaglio, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Minerva Pediatrica|August 31, 1986
[Steinert's dystrophia myotonica . Epidemiological and clinical aspects]M L Mostacciuolo, M Armani
Human Mutation|January 1, 1996
Novel missense mutation of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathyF Schiavon, C Fracasso, M L Mostacciuolo
Gene|October 7, 2003
Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28G Vazza, S Picelli, A Bozzato, et al.
American Journal of Medical Genetics|March 1, 1989
Problems in genetic counseling in a family with an "atypical" centronuclear myopathyB Müller, M L Mostacciuolo, G A Danieli, et al.
Human Mutation|February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypesF Schiavon, A Rampazzo, L Merlini, et al.
Minerva Pediatrica|August 31, 1986
[Genetic counseling in hereditary neuromuscular diseases]G A Danieli, M L Mostacciuolo, P Marchesini, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
American Journal of Medical Genetics|June 15, 1991
Genetic epidemiology of hereditary motor sensory neuropathies (type I)M L Mostacciuolo, G Micaglio, P Fardin, et al.
Neuromuscular Disorders : NMD|October 21, 2006
A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onsetG Vazza, L Merlini, C Bertolin, et al.
Human Genetics|November 1, 1992
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia)E Müller, M L Mostacciuolo, G Micaglio, et al.
Pageof 6