Novel de novo <scp><i>MYRF</i></scp> gene mutation: A possible cause for several clinically overlapping syndromes

• Hiroyuki Tanaka

  Department of Pediatrics, Graduate School of Medicine The University of Tokyo Tokyo Japan

• Tsuyoshi Isojima

  Department of Pediatrics, Graduate School of Medicine The University of Tokyo Tokyo Japan

• Yuki Kimura

  Department of Pediatrics, Graduate School of Medicine The University of Tokyo Tokyo Japan

• Ryo Inuzuka

  Department of Pediatrics, Graduate School of Medicine The University of Tokyo Tokyo Japan

• Sachiko Kitanaka

  Department of Pediatrics, Graduate School of Medicine The University of Tokyo Tokyo Japan

収録刊行物

• Congenital Anomalies

  Congenital Anomalies 61 (2), 68-69, 2020-11-18

  Wiley

キーワード

• Developmental Biology
• Embryology
• General Medicine
• Pediatrics, Perinatology and Child Health

詳細情報

• CRID: 1360567915744872192
• NII論文ID: 210000158651
• DOI: 10.1111/cga.12402
• ISSN: 17414520
• ISSN: 09143505
• Web Site: https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12402
• Web Site: https://onlinelibrary.wiley.com/doi/full-xml/10.1111/cga.12402
• データソース種別:
  • Crossref
  • CiNii Articles
  • KAKEN