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Y L Ko

Showing results (41-50 of 47) with videos related to

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Human Genetics|May 1, 1996
Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failureY L Ko, J J Chen, T K Tang, et al.
Atherosclerosis|December 23, 1998
The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in TaiwanY L Ko, Y S Ko, S M Wang, et al.
Human Genetics|October 1, 1994
No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneityY L Ko, S A Chen, T K Tang, et al.
The American Journal of Cardiology|December 1, 1993
Usefulness of pulmonary venous flow pattern and maximal mosaic jet area detected by transesophageal echocardiography in assessing the severity of mitral regurgitationL P Lai, K G Shyu, J J Chen, et al.
Circulation|August 15, 1995
Transesophageal echocardiographic assessment of mitral valve position and pulmonary venous flow during cardiopulmonary resuscitation in humansM H Ma, J J Hwang, L P Lai, et al.
Human Genetics|August 1, 1996
The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individualsY L Ko, T S Hsu, S M Wu, et al.
Human Genetics|August 1, 1997
Angiotensinogen and angiotensin-I converting enzyme gene polymorphisms and the risk of coronary artery disease in ChineseY L Ko, Y S Ko, S M Wang, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Human Genetics|May 1, 1996
Malignant familial hypertrophic cardiomyopathy in a family with a 453Arg-->Cys mutation in the beta-myosin heavy chain gene: coexistence of sudden death and end-stage heart failureY L Ko, J J Chen, T K Tang, et al.
Atherosclerosis|December 23, 1998
The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in TaiwanY L Ko, Y S Ko, S M Wang, et al.
Human Genetics|October 1, 1994
No evidence for linkage of long QT syndrome and chromosome 11p15.5 markers in a Chinese family: evidence for genetic heterogeneityY L Ko, S A Chen, T K Tang, et al.
The American Journal of Cardiology|December 1, 1993
Usefulness of pulmonary venous flow pattern and maximal mosaic jet area detected by transesophageal echocardiography in assessing the severity of mitral regurgitationL P Lai, K G Shyu, J J Chen, et al.
Circulation|August 15, 1995
Transesophageal echocardiographic assessment of mitral valve position and pulmonary venous flow during cardiopulmonary resuscitation in humansM H Ma, J J Hwang, L P Lai, et al.
Human Genetics|August 1, 1996
The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individualsY L Ko, T S Hsu, S M Wu, et al.
Human Genetics|August 1, 1997
Angiotensinogen and angiotensin-I converting enzyme gene polymorphisms and the risk of coronary artery disease in ChineseY L Ko, Y S Ko, S M Wang, et al.
Pageof 5