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Elizabete Cunha, Celeste Bento, Ana Oliveira, Luís Relvas, Joana Neves, Mariline Gameiro, Cristina Barros, Ana Araújo, Ana Macedo, Paula Rocha, Ricardo Costa, Tabita Maia & M. Letícia Ribeiro. (2013) Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause of α+-Thalassemia in the Portuguese Population. Hemoglobin 37:2, pages 183-187.
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Celeste Bento, Ana Catarina Oliveira, Joana Neves, Mariline Gameiro, Elizabete Cunha, Margarida Coucelo, Ricardo Marques Costa, José Barbot, Emilia Costa, Carlos Fernández-Lago & M. Leticia Ribeiro. (2012) Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a New α-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases. Hemoglobin 36:6, pages 517-525.
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Seyedeh Fatemeh Moosavi, Azam Amirian, Behnaz Zarbakhsh, Alireza Kordafshari, Hasan Mirzahoseini, Sirous Zeinali & Morteza Karimipoor. (2011) The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters. Hemoglobin 35:4, pages 323-330.
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Hamida Mesbah-Amroun, Fatiha Rouabhi, Rolande Ducrocq & Jacques Elion. (2008) Molecular Basis of α-Thalassemia in Algeria. Hemoglobin 32:3, pages 273-278.
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Daniela Santos, Marta Barreto, Irina Kislaya, Joana Mendonça, Miguel P. Machado, Pedro Lopes, Carlos Matias Dias & Paula Faustino. (2023) Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal. Acta Médica Portuguesa 36:7-8, pages 467-474.
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Arun Gurunathan, Cristina Tarango, Patrick T. McGann, Omar Niss & Charles T. Quinn. (2020) Non–transfusion-dependent β-Thalassemia Because of a Single β-Thalassemia Mutation and Coinherited α-Globin Gene Triplication: Need for Increased Awareness to Prevent Incorrect and Delayed Diagnosis. Journal of Pediatric Hematology/Oncology 42:6, pages e494-e496.
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Man-Yu Wu, Jian-Ying Zhou, Jian Li & Dong-Zhi Li. (2015) The Frequency of α-Globin Gene Triplication in a Southern Chinese Population. Indian Journal of Hematology and Blood Transfusion 32:S1, pages 320-322.
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Julio Da Luz, Amalia Ávila, Sandra Icasuriaga, María Gongóra, Luis Castillo, Alejandra Serrón, Elza Miyuki Kimura, Fernando Ferreira Costa, Mónica Sans & Maria de Fátima Sonati. (2013) Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population. Genetics and Molecular Biology 36:3, pages 316-322.
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Gustavo Henrique de Medeiros Alcoforado, Christiane Medeiros Bezerra, Telma Maria Araújo Moura Lemos, Denise Madureira de Oliveira, Elza Miyuki Kimura, Fernando Ferreira Costa, Maria de Fátima Sonati & Tereza Maria Dantas de Medeiros. (2012) Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil. Genetics and Molecular Biology 35:3, pages 594-598.
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Sandrine C. Wagner, Simone M. de Castro, Tatiana P. Gonzalez, Ana P. Santin, Leticia Filippon, Carina F. Zaleski, Laura A. Azevedo, Bruna Amorin, Sidia M. Callegari-Jacques & Mara H. Hutz. (2010) Prevalence of common α-thalassemia determinants in south Brazil: importance for the diagnosis of microcytic anemia. Genetics and Molecular Biology 33:4, pages 641-645.
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Sandrine C. WagnerSimone M. de CastroTatiana P. GonzalezAna Paula SantinCarina F. ZaleskiLaura A. AzevedoHélène DreauShirley HendersonJohn OldMara H. Hutz. (2010) Neonatal Screening for Hemoglobinopathies: Results of a Public Health System in South Brazil. Genetic Testing and Molecular Biomarkers 14:4, pages 565-569.
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María Paulina Nava, Bertha Ibarra, María Teresa Magaña, María de la Luz Chávez & F. Javier Perea. (2006) Prevalence of −α3.7 and αααanti3.7 alleles in sickle cell trait and β-thalassemia patients in Mexico. Blood Cells, Molecules, and Diseases 36:2, pages 255-258.
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B??lent ??zg??nenel & S??reyya Sava??an. (2004) Leftward ?????4.2 Deletion Alpha-Thalassemia in a Patient of Northern European Extraction. Journal of Pediatric Hematology/Oncology 26:1, pages 29-30.
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Wafaa Lemsaddek, Isabel Picanço, Filomena Seuanes, Lahoucine Mahmal, Saâd Benchekroun, Mohammed Khattab, Paulo Nogueira & Leonor Osório‐Almeida. (2003) Spectrum of β thalassemia mutations and HbF levels in the heterozygous Moroccan population. American Journal of Hematology 73:3, pages 161-168.
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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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