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Constitutional mismatch repair deficiency in childhood colorectal cancer harboring a de novo variant in the MSH6 gene: a case report.
Hizuka, Keinosuke; Hagiwara, Shin-Ichiro; Maeyama, Takatoshi; Honma, Hitoshi; Kawai, Masanobu; Akagi, Kiwamu; Yasuhara, Michiko; Tomita, Naohiro; Etani, Yuri.
Afiliação
  • Hizuka K; Department of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan.
  • Hagiwara SI; Department of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan. hagi114@wch.opho.jp.
  • Maeyama T; Department of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan.
  • Honma H; Department of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan.
  • Kawai M; Department of Gastroenterology, Nutrition and Endocrinology, Osaka Women's and Children's Hospital, 840 Murodo-cho, Izumi, Osaka, 594-1101, Japan.
  • Akagi K; Division of Molecular Diagnosis and Cancer Prevention, Saitama Cancer Center, 780, Komuro, Ina-machi, Kitaadachi-gun, Saitama, 780362-0806, Japan.
  • Yasuhara M; Division of Lower GI Surgery, Department of Surgery, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo, 663-8501, Japan.
  • Tomita N; Division of Lower GI Surgery, Department of Surgery, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo, 663-8501, Japan.
  • Etani Y; Cancer Treatment Center, Toyonaka Municipal Hospital, 4-14-1, Shibahara-cho, Toyonaka, Osaka, 560-8565, Japan.
BMC Gastroenterol ; 21(1): 60, 2021 Feb 10.
Article em En | MEDLINE | ID: mdl-33568103
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Neoplasias Encefálicas / Neoplasias Colorretais Tipo de estudo: Prognostic_studies / Screening_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2021 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 / Neoplasias Encefálicas / Neoplasias Colorretais Tipo de estudo: Prognostic_studies / Screening_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article