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2009, ISBN 9812832475, x, 277
Book
Clinical Toxicology, ISSN 1556-3650, 05/2019, Volume 57, Issue 5, pp. 375 - 377
Journal Article
Original Communication - Detection of two rare β-thalassemia mutations [-90 (C → T) and CD 26 (C →T)] among Indians, 12/2005
BACKGROUND: β -Thalassemia (β-thal) is present in practically every caste group in Indians. Molecular characterization of β-thal in these groups has revealed... 
Beta thalassemia | denaturing gradient gel electrophoresis | PCR | India
Journal
BLOOD, ISSN 0006-4971, 10/2019, Volume 134, Issue 14, pp. 1190 - 1193
Abstract Using sickle cell disease as a model, Cutts et al describe a highly sensitive method for prenatal diagnosis of known single-gene defects using... 
FETAL DNA | MATERNAL PLASMA | BETA-THALASSEMIA | HEMATOLOGY
Journal Article
HAEMATOLOGICA, ISSN 0390-6078, 04/2017, Volume 102, pp. 70 - 72
Journal Article
JOURNAL OF MOLECULAR DIAGNOSTICS, ISSN 1525-1578, 07/2019, Volume 21, Issue 4, pp. 572 - 579
During pregnancy, a percentage of the cell-free DNA circulating in the maternal blood is represented by the cell-free fetal DNA (cffDNA), constituting an... 
PATHOLOGY | MATERNAL PLASMA | FEASIBILITY | BETA-THALASSEMIA | PCR
Journal Article
Jornal Brasileiro de Patologia e Medicina Laboratorial, ISSN 1676-2444, 11/2017, Volume 53, Issue 6, pp. 362 - 367
Journal Article
Hematology/Oncology Clinics of North America, ISSN 0889-8588, 06/2019, Volume 33, Issue 3, pp. 339 - 353
Beta thalassemias are a significant global health problem. Globin chain imbalance leads to a complex physiologic cascade of hemolytic anemia, ineffective... 
Iron overload | Chelation | Gene therapy | Beta thalassemia
Journal Article
BLOOD, ISSN 0006-4971, 04/2012, Volume 119, Issue 14, pp. 3263 - 3268
This was a 24-week, multicenter phase-2 study designed to assess safety, tolerability, and pharmacodynamics of FBS0701, a novel oral chelator, in adults with... 
DEFERASIROX ICL670 | THERAPY | BETA-THALASSEMIA | HEMATOLOGY
Journal Article
Current Respiratory Medicine Reviews, ISSN 1573-398X, 12/2016, Volume 12, Issue 4, pp. 277 - 285
Journal Article
Bali Medical Journal, ISSN 2089-1180, 08/2019, Volume 8, Issue 2
Background: The prevalence of  Hb S/β Thalassemia has not been widely reported, and until now, there is a lack of statistical data on the prevalence of the... 
Beta-thalassemia, HbS mutation, Indonesia
Journal Article
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, ISSN 0002-9173, 12/2011, Volume 136, Issue 6, pp. 996 - 997
Journal Article
Pediatric Hematology/Oncology and Immunopathology, ISSN 1726-1708, 2017, Volume 16, Issue 3, pp. 63 - 68
Journal Article
Blood Cells, Molecules, and Diseases, ISSN 1079-9796, 02/2019, Volume 74, pp. 13 - 17
Introduction: Identification of beta-thalassemia carrier in prenatal screening relies on the elevated Hb A level. Borderline Hb A levels pose a diagnostic... 
Beta-thalassemia | Prenatal screening | Thalassemia | Borderline Hb A | Coinherited alpha-thalassemia
Journal Article
Asian Journal of Pharmaceutical and Clinical Research, ISSN 0974-2441, 2018, Volume 11, Issue 11, pp. 467 - 471
Journal Article
Journal Article
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, ISSN 1751-5521, 08/2017, Volume 39, Issue 4, pp. E106 - E109
Journal Article
BLOOD, ISSN 0006-4971, 07/2015, Volume 126, Issue 5, pp. 616 - 619
Globin gene therapy requires abundant numbers of highly engraftable, autologous hematopoietic stem cells expressing curative levels of beta-globin on... 
TERM REPOPULATING CAPACITY | GLOBIN | HEMATOPOIETIC STEM-CELLS | BONE-MARROW | SEVERE BETA-THALASSEMIA | MICE | HEMATOLOGY | TRANSPLANTATION
Journal Article
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