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Luis J. Sánchez-Martínez, Candela L. Hernández, Juan N. Rodríguez, Jean M. Dugoujon, Andrea Novelletto, Paloma Ropero, Luisa Pereira & Rosario Calderón. (2021) Genetic variation patterns of β-thalassemia in Western Andalusia (Spain) reveal a structure of specific mutations within the Iberian Peninsula. Annals of Human Biology 48:5, pages 406-417.
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Licínio Manco, Celeste Bento, Luís Relvas, Elisabete Cunha, Janet Pereira, Valeria Moreira, Manuela Alvarez, Tabita Maia & M. Letícia Ribeiro. (2020) Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers. Hemoglobin 44:2, pages 113-117.
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Juan A. Orts, Ángel Zúñiga, Yanis Bello, Aleix B. Fabregat & Ana I. Vicente. (2016) Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants. Hemoglobin 40:5, pages 335-340.
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Laudy Cherry, Carla Calo, Rodica Talmaci, Pascale Perrin & Lucian Gavrila. (2016) β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area. Hemoglobin 40:2, pages 85-96.
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Maria del Mar Mañú Pereira, Anna Cabot Dalmau & Joan-Lluis Vives Corrons. (2009) Molecular Heterogeneity of β-Thalassemia Alleles in Spain and its Importance in the Diagnosis and Prevention of β-Thalassemia Major and Sickle Cell Disorders. Hemoglobin 33:3-4, pages 226-234.
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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Wafaâ Lemsaddek, Isabel Picanço, Filomena Seuanes, Paulo Nogueira, Lahoucine Mahmal, Saâd Benchekroun, Mohammed Khattab & Leonor Osório‐Almeida. (2004) The β‐Thalassemia Mutation/Haplotype Distribution in the Moroccan Population. Hemoglobin 28:1, pages 25-37.
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Ana Villegas, Paloma Ropero, Fernando A. González, Eduardo Anguita & Domingo Espinós. (2001) THE THALASSEMIA SYNDROMES: MOLECULAR CHARACTERIZATION IN THE SPANISH POPULATION. Hemoglobin 25:3, pages 273-283.
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Articles from other publishers (7)
Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Elvira Mangas-Carrasco & Olalla López-Costas. (2021) Porotic hyperostosis, cribra orbitalia, femoralis and humeralis in Medieval NW Spain. Archaeological and Anthropological Sciences 13:10.
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Leonor Osório Almeida. (2015) Human Gene Mutations and Migratory Flows—Portugal and the Mediterranean. Advances in Anthropology 05:03, pages 164-169.
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Imane AgoutiCatherine BadensAhmed AbouyoubNicolas LevyMohcine Bennani. (2008) Molecular Basis of β-Thalassemia in Morocco: Possible Origins of the Molecular Heterogeneity. Genetic Testing 12:4, pages 563-568.
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Vivian C. D. Reichert, Simone M. de Castro, Sandrine C. Wagner, Dulcinéia M. de Albuquerque, Mara H. Hutz & Sandra Leistner-Segal. (2007) Identification of β thalassemia mutations in South Brazilians. Annals of Hematology 87:5, pages 381-384.
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José Manuel Calvo-Villas, Silvia de la Iglesia Iñigo, Paloma Ropero Gradilla, María Francisca Zapata Ramos, Jorge Cuesta Tovar & Francisco Sicilia Guillén. (2008) Caracterización molecular de la betatalasemia en Lanzarote. Medicina Clínica 130:12, pages 450-452.
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Paula Faustino, Paula Pacheco, Pedro Loureiro, Paulo J. Nogueira & João Lavinha. (2001) The geographic pattern of β‐thalassaemia mutations in the Portuguese population. British Journal of Haematology 107:4, pages 903-904.
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