文献
J-GLOBAL ID:201802250354904521
整理番号:18A0341045
褐色細胞腫/傍神経節腫における標的化次世代配列決定により同定された無症候性遺伝的変化:臨床病理学的相関【Powered by NICT】
Silent genetic alterations identified by targeted next-generation sequencing in pheochromocytoma/paraganglioma: A clinicopathological correlations
著者 (7件):
Pillai Suja
(Cancer Molecular Pathology, School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia)
,
Gopalan Vinod
(Cancer Molecular Pathology, School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia)
,
Lo Chung Y.
(Department of Surgery, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong)
,
Liew Victor
(Department of Surgery, Gold Coast University Hospital, Gold Coast, Australia)
,
Smith Robert A.
(Cancer Molecular Pathology, School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia)
,
Smith Robert A.
(Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Queensland, Australia)
,
Lam Alfred King Y.
(Cancer Molecular Pathology, School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast, Australia)
資料名:
Experimental and Molecular Pathology
(Experimental and Molecular Pathology)
巻:
102
号:
1
ページ:
41-46
発行年:
2017年
JST資料番号:
A1230A
ISSN:
0014-4800
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)