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Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.
Xiong, Fu; Ji, Zhisong; Liu, Yanhui; Zhang, Yu; Hu, Lingling; Yang, Qi; Qiu, Qinwei; Zhao, Lingfeng; Chen, Dong; Tian, Zhihui; Shang, Xuan; Zhang, Leitao; Wei, Xiaofeng; Liu, Cuixian; Yu, Qiuxia; Zhang, Meichao; Cheng, Jing; Xiong, Jun; Li, Dongri; Wu, Xiuhua; Yuan, Huijun; Zhang, Wenqing; Xu, Xiangmin.
Afiliación
  • Xiong F; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Ji Z; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Liu Y; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Zhang Y; Department of Prenatal Diagnosis Center, Maternal and Child Health Hospital, Dongguan, China.
  • Hu L; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Yang Q; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Qiu Q; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Zhao L; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Chen D; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Tian Z; School of Stomatology, Zhengzhou University, Zhengzhou, China.
  • Shang X; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Zhang L; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Wei X; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Liu C; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Yu Q; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Zhang M; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Cheng J; Department of Human Anatomy, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Xiong J; Center for Medical Genetics, Southwest Hospital, Third Military Medical University, Chongqing, China.
  • Li D; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Wu X; Department of Forensic Science, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
  • Yuan H; Department of Orthopedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Zhang W; Center for Medical Genetics, Southwest Hospital, Third Military Medical University, Chongqing, China.
  • Xu X; Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Hum Mutat ; 38(1): 95-104, 2017 01.
Article en En | MEDLINE | ID: mdl-27680507
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Chaperonas Moleculares / Predisposición Genética a la Enfermedad / Displasia de la Dentina / Estudios de Asociación Genética / Genes Dominantes / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Chaperonas Moleculares / Predisposición Genética a la Enfermedad / Displasia de la Dentina / Estudios de Asociación Genética / Genes Dominantes / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos