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Significance of the Multi-gene Panel myRisk in Japan.
Hayashi, Saori; Kubo, Makoto; Matsuzaki, Sawako; Kai, Masaya; Morisaki, Takafumi; Yamada, Mai; Kaneshiro, Kazuhisa; Takao, Yuka; Shimazaki, Akiko; Nagayoshi, Kinuko; Mizuuchi, Yusuke; Nakamura, Masafumi.
Afiliação
  • Hayashi S; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Kubo M; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Matsuzaki S; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; kubo.makoto.804@m.kyushu-u.ac.jp.
  • Kai M; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Morisaki T; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Yamada M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Kaneshiro K; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Takao Y; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Shimazaki A; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Nagayoshi K; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Mizuuchi Y; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Nakamura M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Anticancer Res ; 42(8): 4097-4102, 2022 Aug.
Article em En | MEDLINE | ID: mdl-35896222
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Testes Genéticos 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: Síndromes Neoplásicas Hereditárias / Testes Genéticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article