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Hemoglobin|March 2, 2016
Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland ChinaJian Li, Jin-Mei Yan, Xing-Mei Xie, et al.Hemoglobin|October 3, 2015
Population Screening and Prevention Strategies for Thalassemias and other Hemoglobinopathies of Eastern India: Experience of 18,166 casesTridip Chatterjee, Amit Chakravarty, Sudipa ChakravartyHemoglobin|November 12, 2015
Clinical, Hematological and Molecular Analysis of Homozygous Hb E (HBB: c.79G > A) in the Indian PopulationDivya Jayasree, Ramachandran V Shaji, Biju George, et al.Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, et al.Hemoglobin|August 27, 2014
A local equation for differential diagnosis of β-thalassemia trait and iron deficiency anemia by logistic regression analysis in Southeast IranNarjes Sargolzaie, Ebrahim Miri-MoghaddamHemoglobin|January 1, 1986
Haplotypes of beta S chromosomes among patients with sickle cell anemia from GeorgiaY Hattori, F Kutlar, A Kutlar, et al.Hemoglobin|March 10, 2016
Molecular Characterization of β-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique MutationsMartina Divoka, Martina Partschova, Jana Kucerova, et al.Hemoglobin|March 10, 2016
Sickle Cell Crisis Complicated by Synthetic Cannabinoid Abuse: A Case ReportCrystal Y Zheng, Caterina P Minniti, Mark H ChaitowitzHemoglobin|March 8, 2016
Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest ChinaLuhao Han, Hai Su, Hao Wu, et al.Hemoglobin|February 9, 2016
Symptomatic Erythrocytosis Due to Homozygosity for Hb Luton [HBA2: c.269A>T (or HBA1)] and α-Thalassemia: A Clinical UpdateAmelia Oliveira, Dana Warcel, Nancy Huntley, et al.Pageof 240