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Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis.
Fan, Zhuangzhuang; Sun, Shichen; Liu, Haochen; Yu, Miao; Liu, Ziyuan; Wong, Sing-Wai; Liu, Yang; Han, Dong; Feng, Hailan.
Afiliación
  • Fan Z; Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
  • Sun S; National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, National Clinical Research Center for Oral Diseases, Beijing, China.
  • Liu H; Peking University School and Hospital of Stomatology, Beijing, China.
  • Yu M; Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
  • Liu Z; National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, National Clinical Research Center for Oral Diseases, Beijing, China.
  • Wong SW; Peking University School and Hospital of Stomatology, Beijing, China.
  • Liu Y; Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
  • Han D; National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, National Clinical Research Center for Oral Diseases, Beijing, China.
  • Feng H; Peking University School and Hospital of Stomatology, Beijing, China.
Oral Dis ; 25(8): 2010-2019, 2019 Nov.
Article en En | MEDLINE | ID: mdl-31529555
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Enfermedades Hereditarias del Ojo / Anomalías del Ojo / Proteínas de Homeodominio / Anodoncia / Segmento Anterior del Ojo Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Oral Dis Asunto de la revista: ODONTOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Dinamarca
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Enfermedades Hereditarias del Ojo / Anomalías del Ojo / Proteínas de Homeodominio / Anodoncia / Segmento Anterior del Ojo Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Oral Dis Asunto de la revista: ODONTOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Dinamarca