Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Anemia and HBA2[original query] |
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| First report of the spectrum of d-globin gene mutations in Omani subjects - identification of novel mutations. International journal of laboratory hematology 2015 Apr 37 (2): 238-43. Alkindi S, AlZadjali S, Daar S, Ambusaidi R, Gravell D, Al Haddabi H, Krishnamoorthy R, Pathare |
The genetics of hemoglobin A2 regulation in sickle cell anemia.
American journal of hematology 2014 Nov 89 (11): 1019-23. Griffin Paula J, Sebastiani Paola, Edward Heather, Baldwin Clinton T, Gladwin Mark T, Gordeuk Victor R, Chui David H K, Steinberg Martin |
| Hematological phenotypes in children according to the ?-globin genotypes. Blood cells, molecules & diseases 2017 11 69 102-106. Origa Raffaella, Barella Susanna, Paglietti Maria Elisabetta, Anni Franco, Danjou Fabrice, Denotti Anna Rita, Desogus Maria Franca, Loi Daniela, Orecchia Valeria, Sollaino Maria Carla, Moi Pao |
| The ??3.7 deletion in ??globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population. Molecular medicine reports 2017 11 17 (1): 1879-1884. Borgio J Francis, Abdulazeez Sayed, Almandil Noor B, Naserullah Zaki A, Al-Jarrash Sana, Al-Suliman Ahmed M, Elfakharay Huda Ismail, Qaw Fuad S, Alabdrabalnabi Fatimah I, Alkhalifah Mohammed A, Shakil Akhtar Mohammed, Qutub Hatem, Al-Ali Amein |
| Reference intervals for HbA and HbF and cut-off value of HbA for ?-thalassemia carrier screening in a Guizhou population of reproductive age. Clinical biochemistry 2018 12 65 24-28. Han Wen-Ping, Huang Ling, Li Yuan-Yuan, Han Yuan-Yuan, Li Di, An Bang-Quan, Huang Sheng-W |
| ?-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [?31(B12)Arg?Ser (HBA1 or HBA2 c.96G>T or C)] with the ?-Thalassemia-1 [- - (Southeast Asian)] Deletion in Thailand. Hemoglobin 2020 7 44 (4): 264-271. Panyasai Sitthichai, Phasit Amph |
| Heterozygosity for the Novel HBA2: c.*91_*92delTA Polyadenylation Site Variant on the ?2-Globin Gene Expanding the Genetic Spectrum of ?-Thalassemia in Iran. Hemoglobin 2020 10 44 (6): 423-426. Forouzesh Pour Fatemeh, Karimi Keyvan, Ghaderi Zhila, Tavakoli Koudehi Ameneh, Najmabadi Hosse |
| Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and ?-Major Regulatory Element Haplotype Analysis in Iran. Hemoglobin 2021 3 45 (1): 37-40. Alimohammadi-Bidhendi Sara, Azadmehr Sarah, Razipour Masoumeh, Zeinali Sirous, Eslami Maryam, Davoudi-Dehaghani Elh |
| Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia. Genetics and molecular biology 2021 44 (2): e20200399. Soler Ana María, Piellusch Bruna Facanali, Silveira Lorena da, Pedroso Gisele Audrei, López Pablo, Savio Enrique, Sonati María de Fatima, Luz Julio |
| 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 |
| [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 |
| Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
| Detecting rare thalassemia in children with anemia using third-generation sequencing. Hematology (Amsterdam, Netherlands) 2023 8 28 (1): 2241226. Zhen-Min Ren, Wu-Jiao Li, Zhi-Hao Xing, Xiao-Ying Fu, Ju-Yan Zhang, Yun-Sheng Chen, De-Fa |
| 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 |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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