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Cold Spring Harbor Perspectives in Medicine|May 3, 2013
The molecular basis of β-thalassemiaSwee Lay TheinBritish Journal of Haematology|April 16, 2008
Genetic modifiers of the beta-haemoglobinopathiesSwee Lay TheinJournal of Medical Genetics|February 1, 2020
Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp <i>HBB</i> deletionXunde Wang, Julia Z Xu, Anna Conrey, et al.British Journal of Haematology|November 30, 2006
Molecular therapies in beta-thalassaemiaLynn Quek, Swee Lay TheinBlood|September 13, 2018
How I treat the older adult with sickle cell diseaseSwee Lay Thein, Jo HowardCurrent Opinion in Hematology|February 18, 2017
Genetic control of erythropoiesisLaxminath Tumburu, Swee Lay TheinBritish Journal of Haematology|April 7, 2009
Discovering the genetics underlying foetal haemoglobin production in adultsSwee Lay Thein, Stephan MenzelMolecular Diagnosis & Therapy|November 28, 2018
Genetic Modifiers of Fetal Haemoglobin in Sickle Cell DiseaseStephan Menzel, Swee Lay TheinBritish Journal of Haematology|February 1, 2018
Platelets at the crossroads of thrombosis, inflammation and haemolysisSebastian Vogel, Swee Lay TheinHematology. American Society of Hematology. Education Program|December 7, 2019
Optimal disease management and health monitoring in adults with sickle cell diseaseJo Howard, Swee Lay TheinPageof 23