找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

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

[復制鏈接]
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
 關于派博傳思  派博傳思旗下網站  友情鏈接
派博傳思介紹 公司地理位置 論文服務流程 影響因子官網 吾愛論文網 大講堂 北京大學 Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點評 投稿經驗總結 SCIENCEGARD IMPACTFACTOR 派博系數 清華大學 Yale Uni. Stanford Uni.
QQ|Archiver|手機版|小黑屋| 派博傳思國際 ( 京公網安備110108008328) GMT+8, 2025-10-12 07:26
Copyright © 2001-2015 派博傳思   京公網安備110108008328 版權所有 All rights reserved
快速回復 返回頂部 返回列表
寻甸| 星子县| 抚远县| 彰化市| 安泽县| 鄂伦春自治旗| 靖州| 繁峙县| 纳雍县| 平利县| 乐山市| 泰顺县| 焉耆| 石河子市| 客服| 商河县| 金平| 成安县| 株洲市| 永城市| 基隆市| 衡东县| 江华| 富宁县| 伊通| 昆山市| 留坝县| 伊金霍洛旗| 融水| 台北县| 顺平县| 林州市| 仪陇县| 临高县| 遂宁市| 柳江县| 忻城县| 德保县| 云梦县| 濉溪县| 北票市|