Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: beta-Thalassemia 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 |
HBG2 -158 (C>T) polymorphism and its contribution to fetal hemoglobin variability in Iraqi Kurds with beta-thalassemia minor. Journal of laboratory physicians 2018 12 10 (4): 370-373. Albarawi Dilan J, Balatay Amer A, Al-Allawi Nas |
Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients. Molecular biology reports 2019 11 47 (1): 603-606. AbdulAzeez Sayed, Almandil Noor B, Naserullah Zaki A, Al-Jarrash Sana, Al-Suliman Ahmed M, ElFakharay Huda I, Borgio J Franc |
Evaluation of beta-thalassemia in the fetus through cffDNA with multiple polymorphisms as a haplotype in the beta-globin gene. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2020 Aug . Mirzaei Gisomi Nadia, Javadi Gholamreza, Zare Karizi Shohre, Miryounesi Mohammad, Keshavarz Parvan |
[Effect of high-throughput sequencing for the prevention and control of thalassemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 5 37 (6): 645-649. Chen Yang, Zhang Shufang, Wang Chan, Chen Shiping, Feng Nyu, Liu Haifang, Tang Xiaoyan, Wang J |
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 |
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 |
Clinical significance of mutational variants in beta and alpha genes in patients with hemoglobinopathies from two large Greek centers: a complex interplay between genotype and phenotype. Journal of molecular medicine (Berlin, Germany) 2023 7 . Michael D Diamantidis, Rebecca-Anastasia Karanikola, Chrysoula Polyzoudi, Sophia Delicou, Achilles Manafas, Helen Savera, Aikaterini Xydaki, Angeliki Kotsiafti, Evangelos Tsangalas, Georgia Ikonomou, Eirini Mani, Konstantinos Ntoulas, Evangelos Alexiou, Ioanna Argyrakouli, John Koskinas, Paraskevi Foti |
Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
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- Page last updated:Apr 22, 2024
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