Your browser doesn't support javascript.
loading
Clinical Application of Whole Exome Sequencing to Identify Rare but Remediable Neurologic Disorders.
Kim, Min-Jee; Yum, Mi-Sun; Seo, Go Hun; Lee, Yena; Jang, Han Na; Ko, Tae-Sung; Lee, Beom Hee.
Afiliação
  • Kim MJ; Department of Pediatrics, Asan Medical Center Children's Hospital, Ulsan University College of Medicine 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea.
  • Yum MS; Department of Pediatrics, Asan Medical Center Children's Hospital, Ulsan University College of Medicine 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea.
  • Seo GH; 3billion Inc., Seoul 06193, Korea.
  • Lee Y; Department of Genetics, Asan Medical Center, Ulsan University College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea.
  • Jang HN; Department of Pediatrics, Asan Medical Center Children's Hospital, Ulsan University College of Medicine 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea.
  • Ko TS; Department of Pediatrics, Asan Medical Center Children's Hospital, Ulsan University College of Medicine 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul 05505, Korea.
  • Lee BH; 3billion Inc., Seoul 06193, Korea.
J Clin Med ; 9(11)2020 Nov 20.
Article em En | MEDLINE | ID: mdl-33233562
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Clin Med Ano de publicação: 2020 Tipo de documento: Article