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PAX3/7-FOXO1 fusion-negative alveolar rhabdomyosarcoma in Schuurs-Hoeijmakers syndrome.
Ohkawa, Teppei; Nishimura, Akira; Kosaki, Kenjiro; Aoki-Nogami, Yuki; Tomizawa, Daisuke; Kashimada, Kenichi; Morio, Tomohiro; Kato, Motohiro; Mizutani, Shuki; Takagi, Masatoshi.
Afiliação
  • Ohkawa T; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Nishimura A; Department of Pediatrics, Chiba Kaihinn Municipal Hospital, Chiba, Japan.
  • Kosaki K; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Aoki-Nogami Y; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Tomizawa D; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Kashimada K; Department of Pediatric Oncology, National Cancer Center, Tokyo, Japan.
  • Morio T; Division of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
  • Kato M; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Mizutani S; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.
  • Takagi M; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
J Hum Genet ; 67(1): 51-54, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34341476
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Rabdomiossarcoma Alveolar / Predisposição Genética para Doença / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Rabdomiossarcoma Alveolar / Predisposição Genética para Doença / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article