文献
J-GLOBAL ID:201802281553968302
整理番号:18A0340145
可能な非定型髄膜腫の小児におけるTFG ROS1融合の同定につながるゲノム診断【Powered by NICT】
Genomic diagnostics leading to the identification of a TFG-ROS1 fusion in a child with possible atypical meningioma
著者 (9件):
Rossing Maria
(Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
,
Yde Christina Westmose
(Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
,
Sehested Astrid
(Department of Paediatrics and Adolescent Medicine, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
,
Ostrup Olga
(Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
,
Scheie David
(Department of Pathology, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
,
Dangouloff-Ros Volodia
(Pediatric Imaging Unit, Hopital Necker-Enfants Malades, Paris, France)
,
Geoerger Birgit
(Department of Paediatrics and Adolescent Oncology, Vectorology and Anticancer Therapies, UMR 8203, CNRS, Univ. Paris-Sud, Gustave Roussy, Universite Paris-Saclay, Villejuif, France)
,
Vassal Gilles
(Department of Paediatrics and Adolescent Oncology, Vectorology and Anticancer Therapies, UMR 8203, CNRS, Univ. Paris-Sud, Gustave Roussy, Universite Paris-Saclay, Villejuif, France)
,
Nysom Karsten
(Department of Paediatrics and Adolescent Medicine, Neuroscience Center, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark)
資料名:
Cancer Genetics
(Cancer Genetics)
巻:
212-213
ページ:
32-37
発行年:
2017年
JST資料番号:
T0061A
ISSN:
2210-7762
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
オランダ (NLD)
言語:
英語 (EN)