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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 5
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Original Article

The -87 (C→A) β+-Thalassemia Mutation in a Black Family

M. B. Coleman Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
,
M. H. Steinberg Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
,
A. H. Harrell Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
,
M. W. Plonczynski Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
,
A. M. Walker Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
&
J. G. Adams Department of Veterans Affairs Medical Center and Department of Medicine, University of Mississippi School of Medicine Jackson, MS, 39216, USA
Pages 399-401 | Received 02 Dec 1991, Accepted 11 Jun 1992, Published online: 07 Jul 2009

Citations (11)

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Lei Pan, Peirun Tian, Shiping Chen & Rui Zhang. (2023) Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China. Hemoglobin 47:1, pages 21-24.
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Khushnooma Y. Italia, Pratibha M. Sawant, Anita H. Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2012) Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?. Hemoglobin 36:2, pages 114-123.
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Anita Nadkarni, Ajit Gorakshakar, Reema Surve, Pratibha Sawant, Supriya Phanasgaonkar, Sona Nair, Kanjaksha Ghosh & Roshan B. Colah. (2009) Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population. Hemoglobin 33:1, pages 59-65.
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F. Gümrük, H. Mergen, R. Öner, O. Özcebe, N. Sayinalp, C. Önel, A. Gürgey & Ç. Altay. (2000) β-Thalassemia Intermedia Associated with Homozygosity for the -87 (C→T) Mutation in a Turkish Family. Hemoglobin 24:1, pages 23-29.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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E. Baysal & M. F. H. Carver. (1995) The β- and δ-Thalassemia Repository (Eighth Edition). Hemoglobin 19:3-4, pages 213-236.
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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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T. H. J. Huisman. (1992) The β- and δ-Thalassemia Repository. Hemoglobin 16:4, pages 237-258.
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Articles from other publishers (3)

Gabriella E. Martyn, Kate G.R. Quinlan & Merlin Crossley. (2017) The regulation of human globin promoters by CCAAT box elements and the recruitment of NF-Y. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms 1860:5, pages 525-536.
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Raveen K. Basran, Ulrike M. Reiss, Hong‐yuan Luo, Russell E. Ware & David H.K. Chui. (2006) β‐thalassemia intermedia due to compound heterozygosity for two β‐globin gene promoter mutations, including a novel TATA box deletion. Pediatric Blood & Cancer 50:2, pages 363-366.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .

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