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Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.
Li, Jinliang; Gao, Kai; Yan, Huifang; Xiangwei, Wenshu; Liu, Nana; Wang, Tianshuang; Xu, Han; Lin, Zehong; Xie, Han; Wang, Jingmin; Wu, Ye; Jiang, Yuwu.
Afiliação
  • Li J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Gao K; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Yan H; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Xiangwei W; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Liu N; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang T; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Xu H; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Lin Z; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Xie H; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wu Y; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Jiang Y; Department of Pediatrics, Peking University First Hospital, Beijing, China. Electronic address: jiangyuwu@bjmu.edu.cn.
Gene ; 700: 168-175, 2019 Jun 05.
Article em En | MEDLINE | ID: mdl-30904718
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Epilepsia / Sequenciamento do Exoma / Deficiência Intelectual Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Gene Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Holanda
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Epilepsia / Sequenciamento do Exoma / Deficiência Intelectual Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Gene Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Holanda