Embryonic ζ-Globin Chains in Adults: a Marker for α-Thalassemia-1 Haplotype Due to a >17.5-kb Deletion
Author:
Publisher
Massachusetts Medical Society
Subject
General Medicine
Link
http://www.nejm.org/doi/pdf/10.1056/NEJM198601093140203
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3. LC–MS/MS-Based Absolute Quantitation of Hemoglobin Subunits from Dried Blood Spots Reveals Novel Biomarkers for α-Thalassemia Silent Carriers;Analytical Chemistry;2023-06-07
4. Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--SEA) carriers;Journal of Clinical Pathology;2022-08-25
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