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L L Bachinski

Showing results (21-30 of 28) with videos related to

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Circulation|August 3, 1999
Desmin mutation responsible for idiopathic dilated cardiomyopathyD Li, T Tapscoft, O Gonzalez, et al.
American Journal of Human Genetics|January 13, 2000
The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14D Li, F Ahmad, M J Gardner, et al.
The Journal of Clinical Investigation|May 1, 1990
Molecular cloning, expression, and chromosome 19 localization of a human Ro/SS-A autoantigenD P McCauliffe, F A Lux, T S Lieu, et al.
Circulation|December 15, 1995
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32J B Durand, L L Bachinski, L C Bieling, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
The New England Journal of Medicine|May 1, 1998
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathyH Niimura, L L Bachinski, S Sangwatanaroj, et al.
Circulation|October 31, 2001
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathyD Li, G Z Czernuszewicz, O Gonzalez, et al.
The New England Journal of Medicine|June 16, 2001
Identification of a gene responsible for familial Wolff-Parkinson-White syndromeM H Gollob, M S Green, A S Tang, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Circulation|August 3, 1999
Desmin mutation responsible for idiopathic dilated cardiomyopathyD Li, T Tapscoft, O Gonzalez, et al.
American Journal of Human Genetics|January 13, 2000
The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14D Li, F Ahmad, M J Gardner, et al.
The Journal of Clinical Investigation|May 1, 1990
Molecular cloning, expression, and chromosome 19 localization of a human Ro/SS-A autoantigenD P McCauliffe, F A Lux, T S Lieu, et al.
Circulation|December 15, 1995
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32J B Durand, L L Bachinski, L C Bieling, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
The New England Journal of Medicine|May 1, 1998
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathyH Niimura, L L Bachinski, S Sangwatanaroj, et al.
Circulation|October 31, 2001
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathyD Li, G Z Czernuszewicz, O Gonzalez, et al.
The New England Journal of Medicine|June 16, 2001
Identification of a gene responsible for familial Wolff-Parkinson-White syndromeM H Gollob, M S Green, A S Tang, et al.
Pageof 3