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Rare α(0)-thalassemia deletions detected by MLPA in five unrelated Brazilian patients

Alpha-thalassemias are among the most common genetic diseases in the world. They are characterized by hypochromic and microcytic anemia and great clinical variability, ranging from a practically asymptomatic phenotype to severe anemia, which can lead to intrauterine or early neonatal death. Deletion...

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Detalles Bibliográficos
Autores principales:	Mota, Natália O., Kimura, Elza M., Ferreira, Roberta D., Pedroso, Gisele A., Albuquerque, Dulcinéia M., Ribeiro, Daniela M., Santos, Magnun N. N., Bittar, Cristina M., Costa, Fernando F., Sonati, Maria de Fatima
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Genética 2017
Materias:	Human and Medical Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738609/ https://www.ncbi.nlm.nih.gov/pubmed/28981562 http://dx.doi.org/10.1590/1678-4685-GMB-2016-0330

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