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Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilities.
Suga, Kenichi; Imoto, Issei; Ito, Hiromichi; Naruto, Takuya; Goji, Aya; Osumi, Keita; Tokaji, Narumi; Homma, Yukako; Ono, Akemi; Ichihara, Yuko; Shono, Miki; Mori, Tatsuo; Urushihara, Maki; Nakagawa, Ryuji; Hayabuchi, Yasunobu; Kagami, Shoji.
Afiliación
  • Suga K; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Imoto I; Department of Human Genetics, Graduate school of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
  • Ito H; Division of Molecular Genetics, Aichi Cancer Center Research Institute, Nagoya, Japan.
  • Naruto T; Department of Cancer Genetics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Goji A; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Osumi K; Department of Special Needs Education, Graduate School of Education, Naruto University of Education, Naruto, Japan.
  • Tokaji N; Department of Human Genetics, Graduate school of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
  • Homma Y; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Ono A; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Ichihara Y; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Shono M; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Mori T; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Urushihara M; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Nakagawa R; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Hayabuchi Y; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
  • Kagami S; Department of Pediatrics, Tokushima University Hospital, Tokushima, Japan.
J Med Invest ; 67(3.4): 246-249, 2020.
Article en En | MEDLINE | ID: mdl-33148896
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Secuenciación de Nucleótidos de Alto Rendimiento / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Med Invest Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Japón
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Secuenciación de Nucleótidos de Alto Rendimiento / Discapacidad Intelectual Tipo de estudio: Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Med Invest Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Japón