Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Hemoglobinopathies and MYB[original query] |
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| The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients. Blood cells, molecules & diseases 2010 Aug 45 (2): 124-7. Nguyen Thi Khanh Tien, Joly Philippe, Bardel Claire, Moulsma Mustapha, Bonello-Palot Nathalie, Francina Ala |
| Influences of genetic variation on fetal hemoglobin. Pediatric hematology and oncology 2011 Nov 28 (8): 708-17. He Yunyan, Lin Weixiong, Luo Jianmi |
| Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with ?-Thalassemia and Sickle Cell Disease. Hemoglobin 2018 Mar 42 (2): 103-107. Listì Florinda, Sclafani Serena, Agrigento Veronica, Barone Rita, Maggio Aurelio, D'Alcamo Ele |
| Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine. Scientific reports 2021 Oct 11 (1): 20906. Hariharan Priya, Gorivale Manju, Sawant Pratibha, Mehta Pallavi, Nadkarni Ani |
| Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of tropical pediatrics 2022 9 68 (5): . Rizo-de la Torre L C, Borrayo-López F J, Perea-Díaz F J, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata L L, Ibarra-Cortés |
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- Page last updated:May 22, 2023
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