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Hemoglobin
international journal for hemoglobin research
Volume 11, 1987 - Issue 4
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Original Article

Oligonucleotide Screening of β Thalassemia Mutations in the South East of France

M. Milland Labratoire de Biochimie Médicale, U 38 de I'INSERM and Institut de Pédiatrie, 27, Boulevard Jean Moulin, 13385, Marseille, Cédex 5, France
,
J. L. Bergé-Lefranc Labratoire de Biochimie Médicale, U 38 de I'INSERM and Institut de Pédiatrie, 27, Boulevard Jean Moulin, 13385, Marseille, Cédex 5, France
,
D. Lena Labratoire de Biochimie Médicale, U 38 de I'INSERM and Institut de Pédiatrie, 27, Boulevard Jean Moulin, 13385, Marseille, Cédex 5, France
&
G. Cartouzou Labratoire de Biochimie Médicale, U 38 de I'INSERM and Institut de Pédiatrie, 27, Boulevard Jean Moulin, 13385, Marseille, Cédex 5, France
Pages 317-327 | Published online: 07 Jul 2009

Citations (12)

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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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M. R. Noori-Daloii, N. Moazami, S. Farhangi, A. Atalay, I. N. Geren, L. Akar, E. O. Atalay, B. Clirakoglu & E. Bermek. (1994) β-Thalassemia in iran: A high incidence of the nonsense codon 39 mutation on the island of queshm. Hemoglobin 18:6, pages 449-453.
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A. M. Lossi, M. Milland, J. L. Bergé-Lefranc, D. Lena-Russo & H. Perrimond. (1989) A Further case of β-Thalassemia with an Homozygous T→C Substitution at the Donor Splice Site of the First Intervening Sequence of the β-Globin Gene. Hemoglobin 13:6, pages 619-621.
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Articles from other publishers (9)

Shirley Henderson, Adele Timbs, Janice McCarthy, Alice Gallienne, Margaretha Van Mourik, Gillian Masters, Alison May, Mohamed S.M. Khalil, Anna Schuh & John Old. (2009) Incidence of haemoglobinopathies in various populations — The impact of immigration. Clinical Biochemistry 42:18, pages 1745-1756.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1998) 1 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 1-51.
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Jonathan Flint, Rosalind M. Harding, Anthony J. Boyce & John B. Clegg. (1993) 8 The population genetics of the haemoglobinopathies. Baillière's Clinical Haematology 6:1, pages 215-262.
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A. N. Başak, H. Özçelik, A. Özer, A. Tolun, M. Aksoy, L. Ağaoğlu, F. Ridolfi, L. Ulukutlu, N. Akar, A. Gürgey & B. Kirdar. (1992) The molecular basis of β-thalassemia in Turkey. Human Genetics 89:3, pages 315-318.
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C. Kattamis, H. Hu, G. Cheng, A. L. Reese, J. M. Gonzalez‐Redondo, A. Kutlar, F. Kutlar & T. H. J. Huisman. (2008) Molecular characterization of β‐thalassaemia in 174 Greek patients with thalassaemia major. British Journal of Haematology 74:3, pages 342-346.
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Songsak Petmitr, Prapon Wilairat, Jiraporn Kownkon, Pranee Winichagoon & Suthat Fucharoen. (1989) Molecular basis of βo-thalassemia/HbE disease in Thailand. Biochemical and Biophysical Research Communications 162:2, pages 846-851.
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A Sozuoz, A Berkalp, A Figus, A Loi, M Pirastu & A Cao. (1988) Beta thalassaemia mutations in Turkish Cypriots.. Journal of Medical Genetics 25:11, pages 766-768.
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M C Rosatelli, T Tuveri, M T Scalas, A Di Tucci, G B Leoni, M Furbetta, G Monni & A Cao. (1988) Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populations.. Journal of Medical Genetics 25:11, pages 762-765.
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