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Titlebook: Clinical Cardiogenetics; H.F. Baars,P.A.F.M. Doevendans,J.J. van der Smagt Book 20111st edition Springer-Verlag London Limited 2011

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樓主: brachytherapy
11#
發(fā)表于 2025-3-23 11:28:18 | 只看該作者
Weapon Detection Using PTZ Cameras,Noncompaction of the left ventricle or . (.) is a relatively new clinicopathologic entity, first described by Feldt et al.
12#
發(fā)表于 2025-3-23 17:08:45 | 只看該作者
Representing Position and OrientationIn 2000, Gussak et al. described an idiopathic short QT interval associated with atrial fibrillation in a family and sudden death in an unrelated individual. Three years later, in 2003, Gaita et al. reported the association of a short QT interval and sudden cardiac death in two unrelated European families.
13#
發(fā)表于 2025-3-23 20:57:09 | 只看該作者
14#
發(fā)表于 2025-3-23 23:07:33 | 只看該作者
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. is a disease characterized by progressive fibrofatty replacement of primarily the . (RV). .
15#
發(fā)表于 2025-3-24 05:57:20 | 只看該作者
Noncompaction CardiomyopathyNoncompaction of the left ventricle or . (.) is a relatively new clinicopathologic entity, first described by Feldt et al.
16#
發(fā)表于 2025-3-24 10:29:15 | 只看該作者
Short QT SyndromeIn 2000, Gussak et al. described an idiopathic short QT interval associated with atrial fibrillation in a family and sudden death in an unrelated individual. Three years later, in 2003, Gaita et al. reported the association of a short QT interval and sudden cardiac death in two unrelated European families.
17#
發(fā)表于 2025-3-24 14:25:39 | 只看該作者
18#
發(fā)表于 2025-3-24 18:26:31 | 只看該作者
Joachim von Braun,Heike Baumüllern gathered as a result of the human genome project and large-scale resequencing projects at a rapid pace.. The genetic cause of the vast majority of important monogenic disorders is nowadays known, and more rare disorders are being unraveled quickly. Developments in genomics and sequencing technolog
19#
發(fā)表于 2025-3-24 19:18:53 | 只看該作者
https://doi.org/10.1007/978-3-030-54173-6c aspects of disease. They are specifically trained in communicating the implications of genetic information and genetic disease to patients and their families. In addition, they are trained in syndrome diagnosis and clinical dysmorphology.
20#
發(fā)表于 2025-3-25 02:57:07 | 只看該作者
Ján Chudy,Nestor Popov,Pavel Surynek further study of the disease, and dissections of victims of sudden death revealed bulky hearts. 1 Nowadays, HCM is still a major cause of sudden cardiac death (SCD) in the young, and the most common monogenetic heart disease. . This chapter discusses not only the epidemiology, diagnosis, pathophysi
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