Hemoglobinopathies in Southeast Asia: Molecular biology and clinical medicine

[1] Aswapokee P, 1988, BIRTH DEFECTS, V23, P521

[2] Aung-Than-Batu, 1971, Trop Geogr Med, V23, P23

[3] FUSION OF 2 PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (11) : 1880 - &

[4] HEMOGLOBIN DHONBURI ALPHA-2-BETA-2 126 (H4) VAL-]GLY - A NEW UNSTABLE BETA-VARIANT PRODUCING A BETA-THALASSEMIA INTERMEDIA PHENOTYPE IN ASSOCIATION WITH BETA-0-THALASSEMIA [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1990, 35 (02) : 96 - 99

[5] IDENTIFICATION OF HB LEPORE-WASHINGTON-BOSTON IN ASSOCIATION WITH HB-E [BETA-26(B8)GLU-]LYS] IN A THAI FEMALE [J]. HEMOGLOBIN, 1987, 11 (04) : 309 - 316

[6] THE SPECTRUM OF BETA-THALASSEMIA IN BURMA [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (04) : 574 - 578

[7] Chandrcharoensin-Wilde C, 1988, Birth Defects Orig Artic Ser, V23, P263

[8] CHARACTERIZATION OF 2 DELETIONS THAT REMOVE THE ENTIRE HUMAN ZETA-ALPHA-GLOBIN GENE-COMPLEX (--THAI AND --FIL) [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1988, 70 (02) : 233 - 238

[9] FUCHAROEN G, 1991, BLOOD, V78, P537

[10] MOLECULAR-BASIS OF HBE-BETA-THALASSEMIA AND THE ORIGIN OF HBE IN NORTHEAST THAILAND - IDENTIFICATION OF ONE NOVEL MUTATION USING AMPLIFIED DNA FROM BUFFY COAT SPECIMENS [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) : 698 - 704

[1] Aswapokee P, 1988, BIRTH DEFECTS, V23, P521

[2] Aung-Than-Batu, 1971, Trop Geogr Med, V23, P23

[3] FUSION OF 2 PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (11) : 1880 - &

[4] HEMOGLOBIN DHONBURI ALPHA-2-BETA-2 126 (H4) VAL-]GLY - A NEW UNSTABLE BETA-VARIANT PRODUCING A BETA-THALASSEMIA INTERMEDIA PHENOTYPE IN ASSOCIATION WITH BETA-0-THALASSEMIA [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1990, 35 (02) : 96 - 99

[5] IDENTIFICATION OF HB LEPORE-WASHINGTON-BOSTON IN ASSOCIATION WITH HB-E [BETA-26(B8)GLU-]LYS] IN A THAI FEMALE [J]. HEMOGLOBIN, 1987, 11 (04) : 309 - 316

[6] THE SPECTRUM OF BETA-THALASSEMIA IN BURMA [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (04) : 574 - 578

[7] Chandrcharoensin-Wilde C, 1988, Birth Defects Orig Artic Ser, V23, P263

[8] CHARACTERIZATION OF 2 DELETIONS THAT REMOVE THE ENTIRE HUMAN ZETA-ALPHA-GLOBIN GENE-COMPLEX (--THAI AND --FIL) [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1988, 70 (02) : 233 - 238

[9] FUCHAROEN G, 1991, BLOOD, V78, P537

[10] MOLECULAR-BASIS OF HBE-BETA-THALASSEMIA AND THE ORIGIN OF HBE IN NORTHEAST THAILAND - IDENTIFICATION OF ONE NOVEL MUTATION USING AMPLIFIED DNA FROM BUFFY COAT SPECIMENS [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (02) : 698 - 704