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A clinical and multi­omics study of Van der Woude syndrome in three generations of a Chinese family.
Yang, Kai; Dong, Xing-Yue; Wu, Jue; Zhu, Jian-Jiang; Tan, Ya; Yan, You-Sheng; Lin, Li; Zhang, Dong-Liang.
Afiliación
  • Yang K; Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing 102206, P.R. China.
  • Dong XY; Department of Orthodontics, School of Stomatology, Capital Medical University, Beijing 100050, P.R. China.
  • Wu J; Department of Translational Medicine Laboratory, First Medical Center of People's Liberation Army General Hospital, Beijing 100039, P.R. China.
  • Zhu JJ; Department of Prenatal Diagnosis Center, Haidian Maternal and Child Health Care Hospital, Beijing 100080, P.R. China.
  • Tan Y; Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing 102206, P.R. China.
  • Yan YS; Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing 102206, P.R. China.
  • Lin L; Department of Obstetrics and Gynecology, Peking University International Hospital, Beijing 102206, P.R. China.
  • Zhang DL; Department of Orthodontics, School of Stomatology, Capital Medical University, Beijing 100050, P.R. China.
Mol Med Rep ; 22(4): 2925-2931, 2020 Oct.
Article en En | MEDLINE | ID: mdl-32945398
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Anomalías Múltiples / Composición Familiar / Labio Leporino / Fisura del Paladar / Mutación Missense / Quistes / Factores Reguladores del Interferón / Labio Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mol Med Rep Año: 2020 Tipo del documento: Article Pais de publicación: Grecia
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polimorfismo Genético / Anomalías Múltiples / Composición Familiar / Labio Leporino / Fisura del Paladar / Mutación Missense / Quistes / Factores Reguladores del Interferón / Labio Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mol Med Rep Año: 2020 Tipo del documento: Article Pais de publicación: Grecia