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Journal of Neurology, Neurosurgery, and Psychiatry
|
December 16, 2000
PMP22 related congenital hypomyelination neuropathy
G M Fabrizi, A Simonati, F Taioli, et al.
Biochemical Medicine and Metabolic Biology
|
August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients
G Novelli, M Gennarelli, E Menegazzo, et al.
Neuroepidemiology
|
January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis
M L Mostacciuolo, M Miorin, E Pegoraro, et al.
Journal of Medical Genetics
|
March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms
S Cochrane, J Bergoffen, N D Fairweather, et al.
Molecular Psychiatry
|
September 14, 2006
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26
G Vazza, C Bertolin, E Scudellaro, et al.
Journal of Medical Genetics
|
January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations
M Fanin, D J Duggan, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene
W Kress, E Müller, K Kausch, et al.
Journal of the American College of Cardiology
|
December 1, 1993
Cardiac involvement in Becker muscular dystrophy
P Melacini, M Fanin, G A Danieli, et al.
European Journal of Neurology
|
June 27, 2013
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy
E Gregianin, G Vazza, E Scaramel, et al.
Clinical Endocrinology
|
February 21, 2004
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma
G Opocher, F Schiavi, A Vettori, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 16, 2000
PMP22 related congenital hypomyelination neuropathy
G M Fabrizi, A Simonati, F Taioli, et al.
Biochemical Medicine and Metabolic Biology
|
August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients
G Novelli, M Gennarelli, E Menegazzo, et al.
Neuroepidemiology
|
January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis
M L Mostacciuolo, M Miorin, E Pegoraro, et al.
Journal of Medical Genetics
|
March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms
S Cochrane, J Bergoffen, N D Fairweather, et al.
Molecular Psychiatry
|
September 14, 2006
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26
G Vazza, C Bertolin, E Scudellaro, et al.
Journal of Medical Genetics
|
January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations
M Fanin, D J Duggan, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene
W Kress, E Müller, K Kausch, et al.
Journal of the American College of Cardiology
|
December 1, 1993
Cardiac involvement in Becker muscular dystrophy
P Melacini, M Fanin, G A Danieli, et al.
European Journal of Neurology
|
June 27, 2013
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy
E Gregianin, G Vazza, E Scaramel, et al.
Clinical Endocrinology
|
February 21, 2004
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma
G Opocher, F Schiavi, A Vettori, et al.
Page
of 6