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Imagawa-Matsumoto syndrome: SUZ12-related overgrowth disorder.
Imagawa, Eri; Seyama, Rie; Aoi, Hiromi; Uchiyama, Yuri; Marcarini, Bruno Guimaraes; Furquim, Isabel; Honjo, Rachel Sayuri; Bertola, Debora Romeo; Kim, Chong Ae; Matsumoto, Naomichi.
Afiliación
  • Imagawa E; Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan.
  • Seyama R; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Aoi H; Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan.
  • Uchiyama Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Marcarini BG; Department of Obstetrics and Gynecology, Juntendo University, Tokyo, Japan.
  • Furquim I; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Honjo RS; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan.
  • Bertola DR; Genetics Unit, Instituto da Crianca, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Kim CA; Genetics Unit, Instituto da Crianca, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Matsumoto N; Genetics Unit, Instituto da Crianca, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Clin Genet ; 103(4): 383-391, 2023 04.
Article en En | MEDLINE | ID: mdl-36645289

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Anomalías Craneofaciales / Discapacidad Intelectual Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Anomalías Craneofaciales / Discapacidad Intelectual Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2023 Tipo del documento: Article País de afiliación: Japón