Human Genome Epidemiology Literature Finder
Filtered By: |
Previous |
Records 1 - 5 (of 5 Records) |
Query Trace: Hemoglobinopathies and BCL11A[original query] |
---|
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 Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures. Hematology reports 2017 1 8 (4): 6678. Sclafani Serena, Pecoraro Alice, Agrigento Veronica, Troia Antonio, Di Maggio Rosario, Sacco Massimiliano, Maggio Aurelio, D'Alcamo Elena, Di Marzo Rosal |
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 |
- Page last reviewed:Feb 1, 2024
- Content source: