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Detection of rare and novel gene fusions in patients with diffuse glioma: An institutional retrospective study.

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第一作者： Kentaro,Ohara

第一单位： Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, United States.;Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States.

作者： Kentaro,Ohara ^[1] ; Majd,Al Assaad ^[1] ; Samantha N,McNulty ^[2] ; Hussein,Alnajar ^[3] ; Andrea,Sboner ^[4] ; David C,Wilkes ^[1] ; Feng,He ^[5] ; Jenny Zhaoying,Xiang ^[5] ; Susan,Mathew ^[3] ; Olivier,Elemento ^[6] ; David J,Pisapia ^[1] ; Juan Miguel,Mosquera ^[1]

作者单位： Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, United States.;Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States. ^[1] Invitae, Boulder, CO, United States. ^[2] Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, United States. ^[3] Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, United States.;Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States.;Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, United States.;Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, United States. ^[4] Genomics Resources Core Facility, Weill Cornell Medicine, New York, NY, United States. ^[5] Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States.;Department of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, United States.;Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY, United States. ^[6]

DOI 10.1093/jnen/nlae105

PMID 39340835

发布时间 2025-02-21

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