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Whole genome sequencing of pairwise human subjects reveals DNA mutations specific to developmental dysplasia of the hip.
Zhu, Lun-Qing; Su, Guang-Hao; Dai, Jin; Zhang, Wen-Yan; Yin, Chun-Hua; Zhang, Fu-Yong; Zhu, Zhen-Hua; Guo, Zhi-Xiong; Fang, Jian-Feng; Zou, Cheng-da; Chen, Xing-Guang; Zhang, Ya; Xu, Cai-Ying; Zhen, Yun-Fang; Wang, Xiao-Dong.
Afiliação
  • Zhu LQ; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Su GH; Pediatric Institute of Soochow University, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Dai J; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zhang WY; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Yin CH; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zhang FY; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zhu ZH; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Guo ZX; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Fang JF; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zou CD; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Chen XG; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zhang Y; Pediatric Institute of Soochow University, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Xu CY; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China.
  • Zhen YF; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China. Electronic address: yfzhen@suda.edu.cn.
  • Wang XD; Department of Orthopaedics, Children's Hospital of Soochow University, Suzhou 215000, China. Electronic address: wangxd@suda.edu.cn.
Genomics ; 111(3): 320-326, 2019 05.
Article em En | MEDLINE | ID: mdl-29486210

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Luxação Congênita de Quadril / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Luxação Congênita de Quadril / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article