子女 发表于 2025-3-23 09:53:07
http://reply.papertrans.cn/23/2279/227838/227838_11.pnghallow 发表于 2025-3-23 17:32:40
http://reply.papertrans.cn/23/2279/227838/227838_12.png顶点 发表于 2025-3-23 20:36:46
http://reply.papertrans.cn/23/2279/227838/227838_13.pngMalleable 发表于 2025-3-23 22:24:18
http://reply.papertrans.cn/23/2279/227838/227838_14.png松软无力 发表于 2025-3-24 02:35:48
Restrictive Cardiomyopathyventricular noncompaction. Indeed, an autosomal dominantly segregating cardiomyopathy has been described where a single sarcomere gene mutation caused idiopathic RCM in some and HCM in other family members .退潮 发表于 2025-3-24 09:52:54
http://reply.papertrans.cn/23/2279/227838/227838_16.png者变 发表于 2025-3-24 11:32:11
Brugada Syndromee last 20 years, major advances in clinical and mechanistic knowledge have provided very valuable information about the disease, but remaining questions still propel a large research activity on the subject. In this chapter, we review the present knowledge, on clinical, genetic, and molecular features of BrS.跳脱衣舞的人 发表于 2025-3-24 14:52:54
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nical management and signs are the focus of this practical cardiogenetic reference for those who are involved in the care for cardiac patients with a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic.. . .Th魔鬼在游行 发表于 2025-3-25 02:07:53
https://doi.org/10.1007/978-3-322-89873-9 familial diseases. Both are specifically trained in communicating the implications of genetic information and genetic disease to patients and their families. Clinical geneticists and genetic counsellors often work together with cardiologists to ensure a high standard of care for families with cardiogenetic diseases.