Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Counseling and APOB[original query] |
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Mutation detection in Chinese patients with familial hypercholesterolemia. SpringerPlus 2016 12 5 (1): 2095. Du Ran, Fan Liang-Liang, Lin Min-Jie, He Zhi-Jian, Huang Hao, Chen Ya-Qin, Li Jing-Jing, Xia Kun, Zhao Shui-Ping, Xiang Ro |
Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Oct . Alver Maris, Palover Marili, Saar Aet, Läll Kristi, Zekavat Seyedeh Maryam, Tõnisson Neeme, Leitsalu Liis, Reigo Anu, Nikopensius Tiit, Ainla Tiia, Kals Mart, Mägi Reedik, Gabriel Stacey B, Eha Jaan, Lander Eric S, Irs Alar, Philippakis Anthony, Marandi Toomas, Natarajan Pradeep, Metspalu Andres, Kathiresan Sekar, Esko Tõ |
Targeted Genetic Analysis in a Chinese Cohort of 208 Patients Related to Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2020 Aug . Wang Hao, Yang Hang, Liu Zhaohui, Cui Kai, Zhang Yinhui, Zhang Yujing, Zhao Kun, Yin Kunlun, Li Wenke, Zhou Zh |
Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. BMC genomics 2022 May 23 (1): 385. Feng Yen-Chen A, Stanaway Ian B, Connolly John J, Denny Joshua C, Luo Yuan, Weng Chunhua, Wei Wei-Qi, Weiss Scott T, Karlson Elizabeth W, Smoller Jordan |
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