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Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran.
Alimohammadi-Bidhendi, Sara; Azadmehr, Sarah; Razipour, Masoumeh; Zeinali, Sirous; Eslami, Maryam; Davoudi-Dehaghani, Elham.
Afiliação
  • Alimohammadi-Bidhendi S; Department of Genetics, Faculty of Advanced Technologies in Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
  • Azadmehr S; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
  • Razipour M; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
  • Zeinali S; Department of Genetics, Faculty of Basic Sciences, Shahr-e Rey, Payame Noor University, Tehran, Iran.
  • Eslami M; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
  • Davoudi-Dehaghani E; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Hemoglobin ; 45(1): 37-40, 2021 Jan.
Article em En | MEDLINE | ID: mdl-33775199
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia alfa / Deficiências de Ferro / Anemia Hipocrômica Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Talassemia alfa / Deficiências de Ferro / Anemia Hipocrômica Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article