54 papers found
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KLF1Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin
Prenatal control of nondeletional α -thalassemia: first experience in mainland China : Prenatal control of nondeletional α -thalassemia
Analysis Of δ-Globin Gene Mutations in the Chinese Population
Association of Hb New York with Hb E and α0-Thalassemia in a Chinese Woman Identified by Sebia Capillarys2 System
A Novel α-Thalassemia Frameshift Mutation: Codon 8 (–C)
Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System
Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis
Cord Blood Analysis for Rapid Prenatal Confirmation of Hb Bart’s Disease Using the Sebia Capillary Electrophoresis System
Phenotypic Variability in a Chinese Family with Nondeletional Hb H-Hb Quong Sze Disease
Identification of a New α Chain Variant at Codons 22–25 (–9 nts) Using the Sebia Capillarys 2 Electrophoresis System
Screening for Hb Constant Spring in the Guangdong Province, South China, Using the Sebia Capillary Electrophoresis System
Co-Inheritance of β- and δ-Thalassemia Compromising Prenatal Screening in a Chinese Couple Seeking Prevention
Relationship between insulin resistance and adiponectin expression in a rat model of polycystic ovary syndrome
Mild hemoglobin H-constant spring disease with β-thalassemia—a case report
Detection of Hb Constant Spring by a Capillary Electrophoresis Method
Three Hemoglobin Variants Caused by a Single α-Chain Gene Mutation in a Chinese Family
Hb F-Zhejiang: A Hb F Variant Due to A NovelGγ Mutation [Gγ101(G3)Glu→Gln,GAG>CAG] Detected in a Chinese Newborn
Proposed Screening Criteria for β-Thalassemia Trait During Early Pregnancy in Southern China
A novel mutation of −50 (G→A) in the direct repeat element of the β-globin gene identified in a patient with severe β-thalassemia
Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze
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