Fen Lin, Ph.D.

Affiliations: 
2008 University of Chicago, Chicago, IL 
Area:
General, Journalism, General
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"Fen Lin"

Parents

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Dingxin Zhao grad student 2008 Chicago
 (Turning gray: Transition of political communication in China, 1978--2008.)
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Publications

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Weng MS, Lin F, Zhang JC, et al. (2020) [Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency]. Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition. 51: 252-256
Lin F, Weng MS, Wu JR, et al. (2019) Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification. Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis
Lin F, Yang H, Zhang L, et al. (2019) The analysis of clinical and laboratory data: a large outbreak of dengue fever in Chaozhou, Guangdong province, China. Archives of Virology
Lin F, Lou ZY, Xing SY, et al. (2018) The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China. Gene
Yang H, Wang Q, Zheng L, et al. (2015) Multiple Genetic Modifiers of Bilirubin Metabolism Involvement in Significant Neonatal Hyperbilirubinemia in Patients of Chinese Descent. Plos One. 10: e0132034
Lin M, Jiao JW, Zhan XH, et al. (2014) High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population. Plos One. 9: e102243
Lin M, Zhong TY, Chen YG, et al. (2014) Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China. Plos One. 9: e101505
Lin M, Han ZJ, Wang Q, et al. (2013) Molecular epidemiological survey of hemoglobinopathies in the Wuxi region of Jiangsu Province, eastern China. Hemoglobin. 37: 454-66
Lin M, Wen YF, Wu JR, et al. (2013) Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China. Plos One. 8: e55024
Lin M, Wu JR, Huang Y, et al. (2012) Clinical and molecular characterization of a rare 2.4 kb deletion causing α(+) thalassemia in a Chinese family. Blood Cells, Molecules & Diseases. 49: 83-4
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