Population-based whole-genome sequencing with constrained gene analysis identifies predisposing germline variants in children with central nervous system tumors

MLA

Ulrik Kristoffer Stoltze, et al. Population-Based Whole-Genome Sequencing with Constrained Gene Analysis Identifies Predisposing Germline Variants in Children with Central Nervous System Tumors. Mar. 2022. EBSCOhost, https://doi.org/10.1101/2022.03.01.22271578.

APA

Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Anna Byrjalsen, Astrid Sehested, David Scheie, Torben Stamm Mikkelsen, Simon Rasmussen, Mads Bak, Henrik Okkels, Michael Thude Callesen, Jane Skjøth-Rasmussen, Anne-Marie Gerdes, Kjeld Schmiegelow, René Mathiasen, & Karin Wadt. (2022). Population-based whole-genome sequencing with constrained gene analysis identifies predisposing germline variants in children with central nervous system tumors. https://doi.org/10.1101/2022.03.01.22271578

Chicago

Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, Anna Byrjalsen, Astrid Sehested, David Scheie, Torben Stamm Mikkelsen, et al. 2022. “Population-Based Whole-Genome Sequencing with Constrained Gene Analysis Identifies Predisposing Germline Variants in Children with Central Nervous System Tumors,” March. doi:10.1101/2022.03.01.22271578.