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The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project.
Kim, Man Jin; Kim, Boram; Lee, Heerah; Lee, Jee-Soo; Chae, Seung Won; Shin, Ho Seob; Cho, Sung Im; Kim, Soo Yeon; Moon, Jangsup; Lim, Byung Chan; Ko, Jung Min; Chae, Jong-Hee; Park, Sung Sup; Seong, Moon-Woo.
  • Kim MJ; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Kim B; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Lee H; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Lee JS; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Chae SW; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Shin HS; Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Cho SI; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Kim SY; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Moon J; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Lim BC; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Ko JM; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Chae JH; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • Park SS; Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
  • Seong MW; Department of Pediatrics, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Eur J Hum Genet ; 31(10): 1147-1153, 2023 10.
Article en En | MEDLINE | ID: mdl-37414863
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Raras / Pueblo Asiatico Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Humans País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Raras / Pueblo Asiatico Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Humans País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article