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Mutation analysis of the CYP21A2 gene in congenital adrenal hyperplasia.
Forouzanfar, K; Seifi, M; Hashemi-Gorji, F; Karimi, N; Estiar, M A; Karimoei, M; Sakhinia, E; Karimipour, M; Ghergherehchi, R.
Afiliação
  • Forouzanfar K; Tabriz University of Medical Sciences Department of Medical Genetics, Faculty of Medicine Tabriz Iran.
  • Seifi M; Faculty of Medicine and Dentistry, University of Alberta Department of Medical Genetics Edmonton Canada.
  • Hashemi-Gorji F; Shahid Beheshti University of Medical Sciences Genomic Research Center Tehran Iran.
  • Karimi N; Tabriz University of Medical Sciences Department of Medical Genetics, Faculty of Medicine Tabriz Iran.
  • Estiar MA; Tehran University of Medical Sciences Department of Medical Genetics, School of Medicine Tehran Iran.
  • Karimoei M; Tehran University of Medical Science Department of Clinical Biochemistry Tehran Iran.
  • Sakhinia E; Tabriz University of Medical Sciences Biotechnology Research Center Tabriz Iran mtbious_iums@yahoo.com.
  • Karimipour M; Pasteur Institute of Iran Molecular Medicine Department, Biotechnology Research Center Tehran Iran mortezakarimi@pasteur.ac.ir.
Cell Mol Biol (Noisy-le-grand) ; 61(4): 51-5, 2015 Aug 17.
Article em En | MEDLINE | ID: mdl-26278268
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Predisposição Genética para Doença Tipo de estudo: Prognostic_studies / Screening_studies Limite: Female / Humans / Male Idioma: En Revista: Cell Mol Biol (Noisy-le-grand) Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2015 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteroide 21-Hidroxilase / Hiperplasia Suprarrenal Congênita / Predisposição Genética para Doença Tipo de estudo: Prognostic_studies / Screening_studies Limite: Female / Humans / Male Idioma: En Revista: Cell Mol Biol (Noisy-le-grand) Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2015 Tipo de documento: Article