Rapid separation of human globin chains in normal and thalassemia patients by RP-HPLC

[1]  Z. Rahimi,et al.  The Xmn1 polymorphic site 5′ to the Gγ gene and its correlation to the Gγ:Aγ ratio, age at first blood transfusion and clinical features in β-Thalassemia patients from Western Iran , 2009, Molecular Biology Reports.

[2]  G. Lippi,et al.  Separation of haemoglobin HbE and HbA2 by the fully automated, high‐pressure liquid chromatography Tosoh HLC‐723 G7 analyzer , 2008, International journal of laboratory hematology.

[3]  Z. Rahimi,et al.  Implications of the Genetic Epidemiology of Globin Haplotypes Linked to the Sickle Cell Gene in Southern Iran , 2006, Human biology.

[4]  D. Loukopoulos,et al.  Prenatal diagnosis of β-Thalassemia , 2005, Klinische Wochenschrift.

[5]  P. A. Yapo,et al.  Separation of adult chains of abnormal haemoglobin: Identification by reversed‐phase high‐performance liquid chromatography , 2004, Journal of clinical laboratory analysis.

[6]  Z. Rahimi,et al.  β‐Globin gene cluster haplotypes in sickle cell patients from southwest Iran , 2003, American journal of hematology.

[7]  H. Wajcman Analysis of hemoglobins and globin chains by high-performance liquid chromatography. , 2003, Methods in molecular medicine.

[8]  Y. Wada Advanced analytical methods for hemoglobin variants. , 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[9]  H. Wajcman,et al.  ABNORMAL HEMOGLOBINS: LABORATORY METHODS , 2001, Hemoglobin.

[10]  T. Higgins,et al.  Laboratory investigation of hemoglobinopathies and thalassemias: review and update. , 2000, Clinical chemistry.

[11]  I. Papassotiriou,et al.  Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatography. , 1998, Hemoglobin.

[12]  H. Inoue,et al.  Sensitive detection of human globin chains by microbore high-performance liquid chromatography and its forensic application. , 1997, Journal of chromatography. B, Biomedical sciences and applications.

[13]  Y. Kan,et al.  PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES * , 1980, Annals of the New York Academy of Sciences.

[14]  W. Schroeder,et al.  Preliminary experiments in the separation of globin chains by high performance liquid chromatography. , 1979, Hemoglobin.

[15]  A. Cao,et al.  Prenatal diagnosis of beta-thalassemia. Experience with 24 cases. , 1978, Israel journal of medical sciences.

[16]  J. Hobbins,et al.  Prenatal diagnosis of hemoglobinopathies. A review of 15 cases. , 1976, The New England journal of medicine.

[17]  R. Schneider Differentiation of electrophoretically similar hemoglobins--such as S, D, G, and P; or A2, C, E, and O--by electrophoresis of the globin chains. , 1974, Clinical chemistry.

[18]  W. Schroeder,et al.  THE AMINO ACID SEQUENCE OF THE GAMMA CHAIN OF HUMAN FETAL HEMOGLOBIN. , 1963, Biochemistry.