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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 4, 2023. (Total: 217641Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Syncope and MYH7[original query]
Utility of genetic screening in hypertrophic cardiomyopathy: prevalence and significance of novel and double (homozygous and heterozygous) beta-myosin mutations.
Genetic testing 2003 7 (1): 21-7.
Mohiddin Saidi A, Begley David A, McLam Elisha, Cardoso John-Paul, Winkler Judith B, Sellers James R, Fananapazir Lam
Mutations profile in Chinese patients with hypertrophic cardiomyopathy.
Clinica chimica acta; international journal of clinical chemistry 2005 Jan 351 (1-2): 209-16.
Song Lei, Zou Yubao, Wang Jizheng, Wang Zhimin, Zhen Yisong, Lou Kejia, Zhang Qian, Wang Xiaojian, Wang Hu, Li Jia, Hui Rut
Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy.
The American journal of cardiology 2013 Aug 112 (4): 585-9.
Liu Wen, Liu Wenling, Hu Dayi, Zhu Tiangang, Ma Zhanfeng, Yang Jie, Xie Wenli, Li Cuilan, Li Lei, Yang Jingang, Li Tianchang, Bian Hong, Tong Qigua
[Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy].
Zhonghua xin xue guan bing za zhi 2015 Aug 43 (8): 682-9.
Jie Liu, Wenling Liu, Dayi Hu, Tiangang Zhu, Wen Liu, Zhanfeng Ma, Jie Yang, Wenli Xie, Cuilan Li, Lei Li, Guozhong P
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience.
Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349.
Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C
Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy.
European journal of medical genetics 2019 9 63 (3): 103754.
Robyns Tomas, Breckpot Jeroen, Nuyens Dieter, Vandenberk Bert, Corveleyn Anniek, Kuiperi Cuno, Van Aelst Lucas, Van Cleemput Johan, Willems R
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy.
Forensic science international. Genetics 2021 2 52 102478.
Mori Augusto Akira, Castro Lara Reinel de, Bortolin Raul Hernandes, Bastos Gisele Medeiros, Oliveira Victor Fernandes de, Ferreira Glaucio Monteiro, Hirata Thiago Dominguez Crespo, Fajardo Cristina Moreno, Sampaio Marcelo Ferraz, Moreira Dalmo Antonio Ribeiro, Pachón-Mateos José Carlos, Correia Edileide de Barros, Sousa Amanda Guerra de Moraes Rego, Brión Maria, Carracedo Angel, Hirata Rosario Dominguez Crespo, Hirata Mario Hiroyu
Genetic Analysis of Cardiac Syncope-Related Genes in Korean Patients with Recurrent Neurally Mediated Syncope.
Journal of cardiovascular development and disease 2022 8 9 (8): .
Lee Sung Ho, Park Jong Eun, Ki Chang-Seok, Park Seung-Jung, On Young Keun, Park Kyoung-Min, Kim June S
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