Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran.

Hamid, Mohammad; Ershadi Oskouei, Sanaz; Shariati, Gholamreza; Babaei, Esmaeil; Galehdari, Hamid; Saberi, Alihossein; Sedaghat, Alireza

Hamid, Mohammad; Ershadi Oskouei, Sanaz; Shariati, Gholamreza; Babaei, Esmaeil; Galehdari, Hamid; Saberi, Alihossein; Sedaghat, Alireza.

Afiliação

Hamid M; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran.
Ershadi Oskouei S; Department of Biology, School of Natural Science, University of Tabriz, Tabriz.
Shariati G; Department of Medical Genetics, Faculty of Medicine.
Babaei E; Narges Medical Genetics & PND Laboratory, Kianpars, Ahvaz, Iran.
Galehdari H; Department of Biology, School of Natural Science, University of Tabriz, Tabriz.
Saberi A; Department of Medical Genetics, Faculty of Medicine.
Sedaghat A; Department of Medical Genetics, Faculty of Medicine.

J Pediatr Hematol Oncol ; 40(3): 192-195, 2018 04.

Article em En | MEDLINE | ID: mdl-29420372

Assuntos

Hemoglobina Fetal; Fatores de Transcrição Kruppel-Like/genética; Talassemia beta/genética; Análise Mutacional de DNA; Humanos; Irã (Geográfico); Mutação

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemoglobina Fetal / Talassemia beta / Fatores de Transcrição Kruppel-Like Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Pediatr Hematol Oncol Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article

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