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Biochemical and Biophysical Research Communications
|
April 25, 1996
Fine mapping of the human endothelin-converting enzyme gene by fluorescent in situ hybridization and radiation hybrids
G Albertin, G P Rossi, F Majone, et al.
Human Molecular Genetics
|
September 1, 1997
The preliminary transcript map of a human skeletal muscle
A Pallavicini, R Zimbello, N Tiso, 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.
Genomics
|
November 5, 1997
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
A Rampazzo, A Nava, M Miorin, et al.
Journal of the Neurological Sciences
|
March 10, 1997
Extra-muscle involvement in dystrophinopathies: an electroretinography and evoked potential study
P Girlanda, A Quartarone, R Buceti, et al.
Journal of the Neurological Sciences
|
October 1, 1996
Prognostic factors in mild dystrophinopathies
C Angelini, M Fanin, M P Freda, 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.
Neuromuscular Disorders : NMD
|
March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrier
P Melacini, M Fanin, A Angelini, 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.
Journal of the American College of Cardiology
|
December 29, 2000
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
A Nava, B Bauce, C Basso, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
Biochemical and Biophysical Research Communications
|
April 25, 1996
Fine mapping of the human endothelin-converting enzyme gene by fluorescent in situ hybridization and radiation hybrids
G Albertin, G P Rossi, F Majone, et al.
Human Molecular Genetics
|
September 1, 1997
The preliminary transcript map of a human skeletal muscle
A Pallavicini, R Zimbello, N Tiso, 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.
Genomics
|
November 5, 1997
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
A Rampazzo, A Nava, M Miorin, et al.
Journal of the Neurological Sciences
|
March 10, 1997
Extra-muscle involvement in dystrophinopathies: an electroretinography and evoked potential study
P Girlanda, A Quartarone, R Buceti, et al.
Journal of the Neurological Sciences
|
October 1, 1996
Prognostic factors in mild dystrophinopathies
C Angelini, M Fanin, M P Freda, 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.
Neuromuscular Disorders : NMD
|
March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrier
P Melacini, M Fanin, A Angelini, 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.
Journal of the American College of Cardiology
|
December 29, 2000
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
A Nava, B Bauce, C Basso, et al.
Page
of 10