Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Counseling and LDLR[original query] |
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Novel mutations of low-density lipoprotein receptor gene in China patients with familial hypercholesterolemia. Applied biochemistry and biotechnology 2015 May 176 (1): 101-9. Fan Liang-liang, Lin Min-jie, Chen Ya-qin, Huang Hao, Peng Dao-quan, Xia Kun, Zhao Shui-ping, Xiang Ro |
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 |
A Rare Missense Mutation and a Polymorphism with High Frequency in LDLR Gene among Iranian Patients with Familial Hypercholesterolemia. Advanced biomedical research 2018 3 7 37. Tajamolian Masoud, Kolahdouz Parisa, Nikpour Parvaneh, Forouzannia Seyed Khalil, Sheikhha Mohammad Hasan, Yazd Ehsan Farasha |
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 |
Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients. Human genetics 2020 7 140 (2): 321-331. Horiuchi Yasue, Matsubayashi Hiroyuki, Kiyozumi Yoshimi, Nishimura Seiichiro, Higashigawa Satomi, Kado Nobuhiro, Nagashima Takeshi, Mizuguchi Maki, Ohnami Sumiko, Arai Makoto, Urakami Kenichi, Kusuhara Masatoshi, Yamaguchi K |
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 |
Carrier screening for present disease prevalence and recessive genetic disorder in Taiwanese population. Journal of human genetics 2023 12 . Li Shan Chen, Cheng Wei Yu, Wei Jiun Li, Wen Chi Hsieh, Yi Ping |
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