Misc.

Oct, 2021

小児骨髄不全症候群コホート中のFPD-MMが疑われたRUNX1変異10症例のまとめ(Ten patients with RUNX1 mutation who were suspected with FPD-MM in a pediatric cohort of inherited bone marrow failure syndrome)

日本小児血液・がん学会雑誌
  • Yamamori Ayako
    • ,
  • Hamada Motoharu
    • ,
  • Muramatsu Hideki
    • ,
  • Taniguchi Rieko
    • ,
  • Kataoka Shinsuke
    • ,
  • Kawashima Nozomu
    • ,
  • Narita Atsushi
    • ,
  • Nishio Nobuhiro
    • ,
  • Okuno Yusuke
    • ,
  • Takahashi Yoshiyuki
Volume
58
Number
4
First page
214
Last page
214
Language
English
Publishing type
Publisher
(一社)日本小児血液・がん学会
ID information
  • ISSN : 2187-011X
  • eISSN : 2189-5384
  • Ichushi Web ID : 2022031844
Export
BibTeX RIS
To Misc. list