Animosity
发表于 2025-3-21 17:00:51
书目名称Clinical Cardiogenetics影响因子(影响力)<br> http://impactfactor.cn/2024/if/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics影响因子(影响力)学科排名<br> http://impactfactor.cn/2024/ifr/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics网络公开度<br> http://impactfactor.cn/2024/at/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics网络公开度学科排名<br> http://impactfactor.cn/2024/atr/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics被引频次<br> http://impactfactor.cn/2024/tc/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics被引频次学科排名<br> http://impactfactor.cn/2024/tcr/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics年度引用<br> http://impactfactor.cn/2024/ii/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics年度引用学科排名<br> http://impactfactor.cn/2024/iir/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics读者反馈<br> http://impactfactor.cn/2024/5y/?ISSN=BK0227838<br><br> <br><br>书目名称Clinical Cardiogenetics读者反馈学科排名<br> http://impactfactor.cn/2024/5yr/?ISSN=BK0227838<br><br> <br><br>
aesthetic
发表于 2025-3-21 21:03:22
Zusammenfassung und Handlungsempfehlungen,hies are characterized by incomplete penetrance, meaning that some mutation carriers will remain unaffected during their entire life, and variable expression, i.e. the type and severity of the disease can vary widely, even within families. The availability of diagnostic and management guidelines for
组成
发表于 2025-3-22 02:49:14
https://doi.org/10.1007/978-3-642-56422-2ergo periodic cardiac evaluation for the presence of LVH. In about half of all patients, a disease causing mutation can be detected in one of the genes encoding for sarcomeric proteins. Detection of a disease causing mutation allows predictive genetic testing in relatives, and facilitates identifica
insipid
发表于 2025-3-22 06:40:52
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Enteropathic
发表于 2025-3-22 09:41:23
Christoph Seifarth,Frank L. Dederichsse gene. The nonisolated forms of LVNC are caused by a range of rare genetic defects. Until now, in half of familial isolated LVNC, the genetic defect remains unknown. Genetic defects in a large number of sarcomere and other cardiomyopathy genes and in genes primarily associated with skeletal myopat
STENT
发表于 2025-3-22 14:35:52
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STENT
发表于 2025-3-22 19:59:58
Introduction to Molecular Geneticsilies and populations” section. Although NGS is becoming the most widely used technique to identify mutations, still several other techniques are being applied and in the “Molecular Genetic Techniques” section an overview of all currently used methods is provided. With the use of the aforementioned
指耕作
发表于 2025-3-23 00:56:23
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甜食
发表于 2025-3-23 02:33:49
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强行引入
发表于 2025-3-23 07:57:18
Arrhythmogenic Cardiomyopathynormalities, ventricular arrhythmias with a LBBB morphology, functional and structural alterations of the RV, and fibro-fatty replacement in endomyocardial biopsy. Two-dimensional echocardiography, cineangiography and magnetic resonance are the imaging tools to visualize structural-functional abnorm