Citations (11)
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Read on this site (5)
Nejat Akar & Arm Özden. (1994) Rapid Diagnosis Of Two β-Thalassemia Mutatlons: Frameshift Codon 5 (-CT) And Codon 6 (-A). Pediatric Hematology and Oncology 11:4, pages 459-460.
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T. H. J. Huisman. (1993) The β- and δ-Thalassemia Repository (Seventh Edition). Hemoglobin 17:5, pages 479-499.
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E. George, H-J. Li, Y-J. Fei, A. L. Reese, E. Baysal, B. Cepreganova, J. B. Wilson, L-H. Gu, J. F. Nechtman, T. A. Stoming, J-C. Liu, J. F. Codrington & T. H. J. Huisman. (1992) Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia. Hemoglobin 16:1-2, pages 51-66.
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T. H. J. Huisman. (1992) The β- and δ-Thalassemia Repository. Hemoglobin 16:4, pages 237-258.
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Y. Hattori, Y. Yamashiro, Y. Ohba, T. Miyaji, M. Morishita, Ku. Yamamoto, Ki. Yamamoto, S. Narai & A. Kimura. (1991) A New β-Thalassemia Mutation (Initiation Codon ATG→GTG) Found in the Japanese Population. Hemoglobin 15:4, pages 317-325.
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Articles from other publishers (6)
H. Tamary, S. Surrey, H. Kirschmann, L. Shalmon, R. Zaizov, E. Schwartz & E. F. Rappaport. (2006) Systematic use of automated fluorescence‐based sequence analysis of amplified genomic DNA for rapid detection of point mutations. American Journal of Hematology 46:2, pages 127-133.
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E Fernandez, T Bienvenu, F Desclaux Arramond, K Beldjord, J C Kaplan & C Beldjord. (1993) Use of chemical clamps in denaturing gradient gel electrophoresis: application in the detection of the most frequent Mediterranean beta-thalassemic mutations.. Genome Research 3:2, pages 122-124.
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C. A. Scerri, W. Abela, R. Galdies, M. Pizzuto, J. L. Grech & A. E. Felice. (1993)
The β
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IVS, I-NT no. 6 (T→C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta
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M. L. S. Ribeiro, E. Baysal, F. Kutlar, G. P. Tamagnini, P. Goncalves, D. Lopes & T. H. J. Huisman. (2008) A NOVEL β°‐THALASSAEMIA MUTATION (CODON 15, TGG→TGA) IS PREVALENT IN A POPULATION OF CENTRAL PORTUGAL. British Journal of Haematology 80:4, pages 567-568.
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G. T. Yuuregir, K. Aksoy, M. A. ÇUuruuk, N. Dikmen, Y.‐J. Fei, E. Baysal & T. H. J. Huisman. (2008) Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation. British Journal of Haematology 80:4, pages 527-532.
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Karel Indrak, Vaclav Brabec, Jarmila Indrakova, Ladislav Chrobak, Adriana Sakalova, Marie Jarosova, Jaroslav Cermak, You-jun Fei, Ferdane Kutlar, Yuan-chao Gu, Erol Baysal & Titus H. J. Huisman. (1992) Molecular characterization of β-thalassemia in Czechoslovakia. Human Genetics 88:4, pages 399-404.
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