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Human Molecular Genetics
|
January 1, 1996
A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy
J Milasin, F Muntoni, G M Severini, et al.
Journal of the American College of Cardiology
|
July 10, 1999
Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group
L Mestroni, C Rocco, D Gregori, et al.
Heart (British Cardiac Society)
|
February 21, 1998
Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
F Muntoni, A Di Lenarda, M Porcu, et al.
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of 6
Search research articles
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Showing results (51-60 of 53) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 53 results.
Human Molecular Genetics
|
January 1, 1996
A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy
J Milasin, F Muntoni, G M Severini, et al.
Journal of the American College of Cardiology
|
July 10, 1999
Familial dilated cardiomyopathy: evidence for genetic and phenotypic heterogeneity. Heart Muscle Disease Study Group
L Mestroni, C Rocco, D Gregori, et al.
Heart (British Cardiac Society)
|
February 21, 1998
Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
F Muntoni, A Di Lenarda, M Porcu, et al.
Page
of 6