Titlebook: Cardiovascular Genetics for Clinicians; P. A. Doevendans,A. A. M. Wilde Book 2001 Springer Science+Business Media Dordrecht 2001 DNA.ather

CLAY

thwart

1-83 - 1-161: C2H5NO4.(1/2)DHO - C6H4BrD, LQTS is an inherited disease characterized by prolonged ventricular repolarization and a propensity for life-threatening ventricular tachyarrhythmias resulting in syncope and sudden death [1]. Two forms of inherited long QT syndrome are known: (1) the more common Romano-Ward syndrome (RWS), with an

Genome

1-252 - 1-303: DIO3 - Myoglobin,hat trial made us aware of the complexity of the interaction between antiarrhythmic drugs and factors that control cardiac contractility and rhythm. A balance between structural and ionic components is required for the electromechanical impulse to propagate orderly across the myocardial cells. When

不朽中國(guó)

1.8 Glossary of general abbreviations,ath [1– 3]. The acronym ARVD (Arrhythmogenic Right Ventricular Dysplasia) pointed to the peculiar morphology of the heart in the affected subjects, showing an altered composition of the right ventricular free wall. More recently, the acronym was changed into ARVC (Arrhythmogenic Right Ventricular Ca

SAGE

談判

https://doi.org/10.1007/978-94-010-1019-1DNA; atherosclerosis; cardiovascular; congenital heart disease; diagnostics; genetics; heart; lipoprotein; m

cajole

978-94-010-3888-1Springer Science+Business Media Dordrecht 2001

挑剔為人

Developments in Cardiovascular Medicinehttp://image.papertrans.cn/c/image/221943.jpg

鬧劇

Mets552

Clinical Genetics genetics have led to an increased of diagnostic, prognostic and in some cases even therapeutic possibilities. This progress has also entered cardiology. However, some physicians do not give sufficient information to patients prior to performing a genetic test and not aB other physicians have yet th