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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 1-2
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Original Article

A New Case of Thaiassemia Intemedia: Interaction of a Triplicated α-Globin Locus and β-Thalassemia Trait

A. Villegas Servicio de Hematologia Hospital Universitario San Carlos Universidad Complutense, 28040, Madrid, Spain
,
C. Perez-Clausell Servicio de Hematologia Hospital Txagorri txu, 01009, Vitoria, Spain
,
J. Sanchez Servicio de Hematologia Hospital Universitario San Carlos Universidad Complutense, 28040, Madrid, Spain
&
E. Sal del Rio Servicio de Hematologia Hospital Universitario San Carlos Universidad Complutense, 28040, Madrid, Spain
Pages 99-101 | Received 18 Jun 1991, Accepted 18 Dec 1991, Published online: 07 Jul 2009

Citations (6)

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Read on this site (1)

Paloma Ropero, Ana Villegas, Juan Muñoz, Olga Briceño, Asunción Mora, María Salvador, Marta Polo & Fernando A. González. (2006) First Spanish Case Of Thalassemia Major Due to a Compound Heterozygosity for the IVS-II-848 (C→A) And Codon 39 (C→T) Mutations Of The β-Globin Gene. Hemoglobin 30:1, pages 15-21.
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Articles from other publishers (5)

J.L Vives Corrons. (2001) Anemias por defectos congénitos de la hemoglobina. hemoglobinopatías estructurales y talasemias. Medicine - Programa de Formación Médica Continuada Acreditado 8:51, pages 2684-2693.
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S. L. Rhodes, M. Plonczynski, A. Harrell, J. Li, S. Safaya, J. C. Files & M. H. Steinberg. (1999) Double Heterozygosity for the Codon ?? 39 C-to-T Nonsense Mutation and a Triplicate ??-Globin Gene Locus Can Cause ???Dominantly??? Inherited ??-Thalassemia Intermedia. The American Journal of the Medical Sciences 317:5, pages 341.
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S.L. Rhodes, M. Plonczynski, A. Harrell, J. Li, S. Safaya, J.C. Files & M.H. Steinberg. (1999) Double Heterozygosity for the Codon β 39 C-to-T Nonsense Mutation and a Triplicate α-Globin Gene Locus Can Cause "Dominantly" Inherited β-Thalassemia Intermedia. The American Journal of the Medical Sciences 317:5, pages 341-345.
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C. Camaschella, A.C. Kattamis, D. Petroni, A. Roetto, P. Sivera, L. Sbaiz, A. Cohen, K. Ohene-Frempong, P. Trifillis, S. Surrey & P. Fortina. (1997) Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia. American Journal of Hematology 55:2, pages 83-88.
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Gurjevan Garewal, Clair W. Fearon, Tina C. Warren, Neelam Marwaha, Ram K. Marwaha, Chitra Mahadik & Haig H. KazazianJrJr. (2008) The molecular basis of β thalassaemia in Punjabi and Maharashtran Indians includes a multilocus aetiology involving triplicated α‐globin loci. British Journal of Haematology 86:2, pages 372-376.
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