Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Thalassemia and HPFH[original query] |
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| The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity. BMC medical genetics 2010 11 (1): 31. Chen Wanqun, Zhang Xinhua, Shang Xuan, Cai Ren, Li Liyan, Zhou Tianhong, Sun Manna, Xiong Fu, Xu Xiangm |
| KLF1 gene mutations in Chinese adults with increased fetal hemoglobin. Hemoglobin 2013 37 (5): 501-6. Wang Ting, He Yi, Zhou Jian-Ying, Xie Xing-Mei, Li Jian, Li Ru, Liao Can, Li Dong-Z |
| Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results. Hemoglobin 2013 37 (4): 359-68. Belhoul Khawla M, Abdulrahman Mahera, Alraei Rafeeiah |
| Molecular Epidemiological Investigation of Thalassemia in the Chengdu Region, Sichuan Province, Southwest China. Hemoglobin 2015 Aug 1-5. Yu Xia, Yang Li-Ye, Yang Hui-Tian, Liu Cheng-Gui, Cao Deng-Cheng, Shen Wei, Yang Hui, Zhan Xiao-Fen, Li Jian, Xue Bing-Rong, Lin M |
| [Genotype Analysis of Hemoglobinopathy in Chinese Jiangsu Population]. Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2015 Dec 23 (6): 1742-8. Wang Wen-Juan, Xie Jun-Dan, Wang Qian, Tao Ting-Ting, Yao Hong, Wen Li-Jun, Zhou You-Ning, Chen Su-Ni |
| The prevalence and molecular characterization of (??) -thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population. Journal of clinical laboratory analysis 2017 8 32 (3): . He Sheng, Wei Yuan, Lin Li, Chen Qiuli, Yi Shang, Zuo Yangjin, Wei Hongwei, Zheng Chenguang, Chen Biyan, Qiu XiaoX |
| [Rare thalassemia mutations among southern Chinese population]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 12 34 (6): 792-796. Lin Fen, Yang Liye, Lin Min, Zheng Xiangbian, Lu Min, Qiu Meilan, Li Liejun, Xie Long |
| Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India. Hematology (Amsterdam, Netherlands) 2018 Apr 1-5. Pandey Hareram, Ranjan Ravi, Singh Kanwaljeet, Sharma Amit, Kishor Kamal, Seth Tulika, Saxena Re |
| A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as ?-Thalassemia Intermedia Due to a KLF1 Gene Mutation. Hemoglobin 2019 6 43 (2): 140-144. Yang Kun, Ren Quan, Wu Yi, Zhou Yali, Yin Xiaol |
| Molecular analysis of ?-thalassemia and ?-thalassemia in Quanzhou region Southeast China. Journal of clinical pathology 2019 10 73 (5): 278-282. Zhuang Jianlong, Jiang Yuying, Wang Yuanbai, Zheng Yu, Zhuang Qianmei, Wang Junyu, Zeng Shuho |
| The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of ß-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. Hemoglobin 2020 Jul 1-9. Genc Ahmet, Tastemir Korkmaz Deniz, Bayram Suleyman, Rencuzogullari Eyy |
| Key Determinants of Phenotypic Heterogeneity of Hb E/? Thalassemia: A Comparative Study from Eastern India. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2020 3 36 (1): 123-128. Kalantri Siddhesh Arun, Ray Rudra, Choudhuri Soumita, Roy Swarnalata, Bhattacharyya Maitrey |
| Evaluation of intervention strategy of thalassemia for couples of childbearing ages in Centre of Southern China. Journal of clinical laboratory analysis 2021 9 35 (10): e23990. Jiang Fan, Zuo Liandong, Li Jian, Chen Guilan, Tang Xuewei, Zhou Jianying, Qu Yanxia, Li Dongzhi, Liao C |
| Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
| Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients. Genetic testing and molecular biomarkers 2021 3 25 (3): 247-252. Rizo-de la Torre Lourdes Del Carmen, Rentería-López Víctor Manuel, Sánchez-López Josefina Yoaly, Magaña-Torres María Teresa, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javi |
| [Molecular Epidemiological Characteristics and Differential Diagnosis of Common ??-Thalassemia/HPFH]. Zhongguo shi yan xue ye xue za zhi 2022 8 30 (4): 1182-1187. Ju Ai-Ping, Li Na, Lin Keng, Huang Hui-Hui, Liu Shu-Xian, Jiang F |
| SNPscan Combined With CNVplex as a High-Performance Diagnostic Method for Thalassemia. Prenatal diagnosis 2024 9 . Xiaofeng Wei, Xingmin Wang, Fu Xiong, Xinhua Zhang, Dun Liu, Wanjun Zhou, Fei He, Xuan Sha |
| [Analysis of rare mutations associated with Thalassemia and their hematological characteristics in Chenzhou region of Hunan Province]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 5 41 (6): 708-714. Caiyun Li, Jian Zhang, Yingli Cao, Haoqing Zhang, Dongqun Huang, Jufang Tan, Shuai Hou, Dongzhu L |
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