Your browser doesn't support javascript.
loading
Genetic mutation analysis in Japanese patients with non-syndromic congenital heart disease.
Yoshida, Akiko; Morisaki, Hiroko; Nakaji, Mai; Kitano, Masataka; Kim, Ki-Sung; Sagawa, Koichi; Ishikawa, Shiro; Satokata, Ichiro; Mitani, Yoshihide; Kato, Hitoshi; Hamaoka, Kenji; Echigo, Shigeyuki; Shiraishi, Isao; Morisaki, Takayuki.
Afiliación
  • Yoshida A; Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
  • Morisaki H; Department of Medical Genetics, National Cerebral and Cardiovascular Center, Suita, Japan.
  • Nakaji M; Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
  • Kitano M; Department of Medical Genetics, National Cerebral and Cardiovascular Center, Suita, Japan.
  • Kim KS; Department of Molecular Pathophysiology, Osaka University Graduate School of Pharmaceutical Sciences, Suita, Japan.
  • Sagawa K; Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute, Suita, Japan.
  • Ishikawa S; Department of Molecular Pathophysiology, Osaka University Graduate School of Pharmaceutical Sciences, Suita, Japan.
  • Satokata I; Department of Pediatric Cardiology, National Cerebral and Cardiovascular Center, Suita, Japan.
  • Mitani Y; Division of Cardiology, National Center for Child Health and Development, Tokyo, Japan.
  • Kato H; Department of Pediatric Cardiology, Fukuoka Children's Hospital Medical Center, Fukuoka, Japan.
  • Hamaoka K; Department of Pediatric Cardiology, Fukuoka Children's Hospital Medical Center, Fukuoka, Japan.
  • Echigo S; Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Shiraishi I; Department of Pediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
  • Morisaki T; Division of Cardiology, National Center for Child Health and Development, Tokyo, Japan.
J Hum Genet ; 61(2): 157-62, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26490186
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas / Mutación Tipo de estudio: Prognostic_studies País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas / Mutación Tipo de estudio: Prognostic_studies País/Región como asunto: Asia Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article