Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Counseling and HBA2[original query] |
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[Study on the incidence of beta-Thalassemia and genotypes among children under 7 year-olds in Nanning, Liuzhou and Baise areas, Guangxi province]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2009 Oct 30 (10): 1021-4. Qiu Xiao-qiang, Chen Ping, Zhang Ning, Zeng Xiao-yun, Huang Cai-qian, Chen Wen-qiang, Lin Wei-xiong, Li Shu-qu |
[Prevalence and molecular analysis of ß-thalassemia in children of Han ethnicity in Chongqing city]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2013 Jul 51 (7): 7. Yao XY, Zhang YM, Qin ZZ, Fan R, Zou L, Chen SP, Zhang L, Xie Q, Zhong XY, Xian Y, Yu J |
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 |
The Prevalence and Spectrum of a-Thalassemia in Guizhou Province of South China. Hemoglobin 2015 39 (4): 260-3. Huang Sheng-Wen, Xu Yin, Liu Xing-Mei, Zhou Man, Li Gui-Fang, An Bang-Quan, Su Li, Wu Xian, Lin Ji |
A Comprehensive Molecular Investigation of a-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 2017 Jan 41 (1): 32-37. Eftekhari Hajar, Tamaddoni Ahmad, Mahmoudi Nesheli Hassan, Vakili Mohsen, Sedaghat Sadegh, Banihashemi Ali, Azizi Mandana, Youssefi Kamangar Reza, Akhavan-Niaki Hal |
The Spectrum of ?-Thalassemia Mutations in the Lak Population of Iran. Hemoglobin 2019 7 43 (2): 107-111. Moradi Keivan, Aznab Mozaffar, Tahmasebi Susan, Dastafkan Zahra, Omidniakan Leila, Ahmadi Mahsa, Alibakhshi Re |
Genetic epidemiology of beta-thalassemia in the Maldives: 23 years of a beta-thalassemia screening program. Gene 2020 3 741 144544. Mustafa Ibrahim, Firdous Naila, Shebl Fatma M, Shi Zumin, Saeed Mariya, Zahir Zileena, Zayed Hat |
HV2 fragment mutations in ?-thalassemia patients and a new base pair insertion of high-altitude cases. American journal of blood research 2020 11 10 (5): 283-293. Al Thwiby Nsreen M, Hussien Nahed A, Bayoumy Eman S, Shokary Mohamm |
Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals. Hemoglobin 2021 4 45 (1): 49-51. Liu Li, Sun Yan, Chen Shiping, Yu Churen, Cao Peijie, Sun Jun, Peng Zhiyu, Mao Pi |
[A case with ?-thalassemia caused by novel start codon variant in conjunct with right deletion variant of ?2-globin gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 1 38 (1): 12-14. Chen Yang, Wang Jie, Wang Chan, Chen Shiping, Feng Nyu, Liu Haifang, Tang Xiaoyan, Zhang Shufa |
[Genotypic and hematological characteristics of 83 ?-thalassemia mutation carriers and patients from Henan Province]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 7 39 (7): 674-679. Wang Weilin, Zhao Xiaoming, Bai Songting, Wang Lu, Wang Chunmei, Yao Qianghua, Li Bai, Wang D |
The frequency of HK?? allele in silent deletional ?-thalassemia carriers in the Yulin region of southern China using the third-generation sequencing. Gene 2023 5 875 147505. Sisi Ning, Yunrong Qin, Yunning Liang, Yi Liang, Yuling Xie, Yinghong Lu, Guanghong Wei, Ruofan Xu, Yinyin Liu, Jihui |
Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
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- Page last updated:Mar 25, 2024
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