Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China

Molecular Genetics & Genomic Medicine

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[1] Department of Hematology, The First People’s Hospital of Yunnan Province, Kunming, China;Department of Obstetrics and Gynecology, The First People’s Hospital of Yunnan Province, Kunming, China;Genetic Diagnosis Center, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People’s Hospital of Yunnan Province, Kunming, China;Affiliated Hospital of Kunming University of Science and Technology, Kunming, China;Department of Obstetrics and Gynecology, The First People’s Hospital of Yunnan Province, Kunming, China;Genetic Diagnosis Center, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People’s Hospital of Yunnan Province, Kunming, China;Affiliated Hospital of Kunming University of Science and Technology, Kunming, China;Department of Hematology, The First People’s Hospital of Yunnan Province, Kunming, China;Genetic Diagnosis Center, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People’s Hospital of Yunnan Province, Kunming, China;Genetic Diagnosis Center, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People’s Hospital of Yunnan Province, Kunming, China;Affiliated Hospital of Kunming University of Science and Technology, Kunming, China;

关键词: bioinformatics analysis;    capillary electrophoresis;    hereditary persistence of fetal hemoglobin;    δ‐thalassemia;   

DOI  :  10.1002/mgg3.706

来源: publisher

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