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British Heart Journal
|
February 1, 1993
Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy
S al-Mahdawi, S Chamberlain, J Cleland, et al.
Human Molecular Genetics
|
August 1, 1995
Friedreich's ataxia: a defect in signal transduction?
J J Carvajal, M A Pook, K Doudney, et al.
Cardiovascular Research
|
July 1, 1993
Parathyroid hormone related peptide gene expression in human fetal and adult heart
T D Bui, A Shallal, A N Malik, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene
E Dausse, M Komajda, L Fetler, et al.
British Heart Journal
|
August 1, 1994
The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene
S al-Mahdawi, S Chamberlain, L Chojnowska, et al.
The American Journal of Cardiology
|
October 1, 1995
The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy
M P Ryan, J G Cleland, J A French, et al.
Journal of Molecular and Cellular Cardiology
|
February 1, 1997
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
F Tesson, C Dufour, J C Moolman, et al.
Neurogenetics
|
November 21, 2001
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis
M A Pook, S Al-Mahdawi, C J Carroll, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 18 results.
British Heart Journal
|
February 1, 1993
Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy
S al-Mahdawi, S Chamberlain, J Cleland, et al.
Human Molecular Genetics
|
August 1, 1995
Friedreich's ataxia: a defect in signal transduction?
J J Carvajal, M A Pook, K Doudney, et al.
Cardiovascular Research
|
July 1, 1993
Parathyroid hormone related peptide gene expression in human fetal and adult heart
T D Bui, A Shallal, A N Malik, et al.
The Journal of Clinical Investigation
|
December 1, 1993
Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene
E Dausse, M Komajda, L Fetler, et al.
British Heart Journal
|
August 1, 1994
The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene
S al-Mahdawi, S Chamberlain, L Chojnowska, et al.
The American Journal of Cardiology
|
October 1, 1995
The standard electrocardiogram as a screening test for hypertrophic cardiomyopathy
M P Ryan, J G Cleland, J A French, et al.
Journal of Molecular and Cellular Cardiology
|
February 1, 1997
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
F Tesson, C Dufour, J C Moolman, et al.
Neurogenetics
|
November 21, 2001
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis
M A Pook, S Al-Mahdawi, C J Carroll, et al.
Page
of 2