t(8;12;21)を伴うRUNX1-RUNX1T1白血病の症例におけるCohen症候群の原因遺伝子であるVPS13Bの再配列

ABE Akihiro; YAMAMOTO Yukiya; KATSUMI Akira; OKAMOTO Akinao; TOKUDA Masutaka; INAGUMA Yoko; YAMAMOTO Kiyoko; YANADA Masamitsu; KANIE Tadaharu; TOMITA Akihiro; AKATSUKA Yoshiki; OKAMOTO Masataka; KAMEYAMA Toshiki; MAYEDA Akila; EMI Nobuhiko

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J-GLOBAL ID：201802219296119089 整理番号：18A1570665

t(8;12;21)を伴うRUNX1-RUNX1T1白血病の症例におけるCohen症候群の原因遺伝子であるVPS13Bの再配列

Rearrangement of VPS13B, a causative gene of Cohen syndrome, in a case of RUNX1-RUNX1T1 leukemia with t(8;12;21)

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著者 (15件)： , , , , , , , , , , , , , ,
資料名：
巻： 108 号： 2 ページ： 208-212 発行年： 2018年08月
JST資料番号： F0888A ISSN： 0925-5710 CODEN： IJHEEY 資料種別：逐次刊行物 (A)
記事区分：原著論文発行国：ドイツ (DEU) 言語：英語 (EN)

・RUNX1-RUNX1T1融合遺伝子を伴う急性骨髄性白血病...

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血液の腫よう , 先天性疾患・奇形一般

引用文献 (21件)：

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