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Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey.
Demir, Selma; Yalçintepe, Sinem; Atli, Emine Ikbal; Sanri, Aslihan; Yildirim, Ruken; Tütüncüler, Filiz; Çelik, Mehmet; Atli, Engin; Özemri Sag, Sebnem; Eker, Damla; Temel, Sehime; Gürkan, Hakan.
Afiliación
  • Demir S; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Yalçintepe S; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Atli EI; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Sanri A; Department of Pediatrics, Samsun Ondokuz Mayis Üniversitesi, Samsun, Turkey.
  • Yildirim R; Department of Pediatric Endocrinology, Diyarbakir Hospital of Pediatric Diseases, Diyarbakir, Turkey.
  • Tütüncüler F; Department of Pediatric Endocrinology and Trakya University Faculty of Medicine, Edirne, Turkey.
  • Çelik M; Department of Endocrinology, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Atli E; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Özemri Sag S; Department of Medical Genetics, Faculty of Medicine, Uludag University, Bursa, Turkey.
  • Eker D; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
  • Temel S; Department of Medical Genetics, Faculty of Medicine, Uludag University, Bursa, Turkey.
  • Gürkan H; Department of Medical Genetics, Trakya University Faculty of Medicine, Edirne, Turkey.
Genet Test Mol Biomarkers ; 25(1): 59-67, 2021 Jan.
Article en En | MEDLINE | ID: mdl-33470886
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Mutación Missense / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Genet Test Mol Biomarkers Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Mutación Missense / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Genet Test Mol Biomarkers Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Estados Unidos