Your browser doesn't support javascript.
loading
Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T-ARMS-PCR assay.
Jalessi, Maryam; Gholami, Mohammad Saeed; Razmara, Ehsan; Hassanzadeh, Sajad; Sadeghipour, Alireza; Jahanbakhshi, Amin; Tabibkhooei, Alireza; Bahrami, Eshagh; Falah, Masoumeh.
Afiliação
  • Jalessi M; Skull Base Research Center, The Five Senses Health Institute, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Gholami MS; ENT and Head and Neck Research Center and Department, The Five Senses Health Institute, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Razmara E; Skull Base Research Center, The Five Senses Health Institute, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Hassanzadeh S; Department of Hematology and Blood Transfusion, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Sadeghipour A; Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
  • Jahanbakhshi A; Skull Base Research Center, The Five Senses Health Institute, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Tabibkhooei A; Pathology Department, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Bahrami E; Skull Base Research Center, The Five Senses Health Institute, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Falah M; Department of Neurosurgery, Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
J Clin Lab Anal ; 36(1): e24150, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34837714

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cordoma / Predisposição Genética para Doença / Proteínas com Domínio T / Polimorfismo de Nucleotídeo Único / Proteínas Fetais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cordoma / Predisposição Genética para Doença / Proteínas com Domínio T / Polimorfismo de Nucleotídeo Único / Proteínas Fetais Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article