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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 5-6
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Original Article

Newer Developments in the Identification of β-Thalasseuia

T. A. Stoming Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. C. Diaz-chico Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
K. G. Yang Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
D. G. Efremov Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H. J. Huisman Department of Cell and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 565-576 | Received 18 Dec 1987, Accepted 01 Jun 1988, Published online: 07 Jul 2009

Citations (9)

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Ilhem Ben Charfeddine, Taheni Ben Lazreg, Ahlem M’sakni, Abdelbasset Amara, Adnène Mlika, Anouar Chaïeb, Khalid Hlel, Noura Zouari, Faïza Zbidi, Jihène Bouguila, Najla Soyah, Abdelkarim Ayedi, Hechmi Ben Hamouda, Saoussen Abroug, Lamia Boughamoura, Ali Saad & Moez Gribaa. (2015) Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population. Hemoglobin 39:4, pages 251-255.
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H-J. Li, W-Z. Yu, C-H. Zhou, X-J. Hao & Y. Zhou. (1993) The β-Thalassemia Frameshift at Codon 8 (-AA) Observed in four Chinese of the Uygur Nationality. Hemoglobin 17:6, pages 537-541.
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C. Wildmann, Y. Larondelle, J. L. Vaerman, R. Eeckels, P. Martiat & M. Philippel. (1993) An Initiation Codon Mutation as a Cause of β-Thalassemia in a Belgian Family. Hemoglobin 17:1, pages 19-30.
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Bruno Masala. (1992) Hemoglobinopathies in Sardinia. Hemoglobin 16:4, pages 331-351.
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D. G. Efremov, A. J. Dimovski & G. D. Efremov. (1991) Detection of β-Thalassemia Mutations by Aso Hybridization of PCR Amplified DNA With Digoxigenin ddUTP Labeled Oligonucleotides. Hemoglobin 15:6, pages 525-533.
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Articles from other publishers (4)

Wen Wang, Shirley K Y Kham, Gare-Hoon Yeo, Thuan-Chong Quah & Samuel S Chong. (2003) Multiplex Minisequencing Screen for Common Southeast Asian and Indian β-Thalassemia Mutations. Clinical Chemistry 49:2, pages 209-218.
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C. A. Scerri, W. Abela, R. Galdies, M. Pizzuto, J. L. Grech & A. E. Felice. (1993) The β + IVS, I-NT no. 6 (T→C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta . British Journal of Haematology 83:4, pages 669-671.
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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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J. G. Hendy & M. N. Cauchi. (2006) Direct detection of β thalassemic mutations: Use of biotin‐labelled allele specific probes. American Journal of Hematology 34:2, pages 151-153.
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