1. Absence of KMT2D/MLL2 mutations in abdominal paraganglioma. (22nd September 2015) Authors: Stenman, Adam; Juhlin, Carl C.; Haglund, Felix; Brown, Taylor C.; Clark, Victoria E.; Svahn, Fredrika; Bilguvar, Kaya; Goh, Gerald; Korah, Reju; Lifton, Richard P.; Carling, Tobias Journal: Clinical endocrinology Issue: Volume 84:Number 4(2016) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene. Issue 9 (29th May 2015) Authors: Juhlin, C. Christofer; Stenman, Adam; Haglund, Felix; Clark, Victoria E.; Brown, Taylor C.; Baranoski, Jacob; Bilguvar, Kaya; Goh, Gerald; Welander, Jenny; Svahn, Fredrika; Rubinstein, Jill C.; Caramuta, Stefano; Yasuno, Katsuhito; Günel, Murat; Bäckdahl, Martin; Gimm, Oliver; Söderkvist, Peter; ... Journal: Genes, chromosomes & cancer Issue: Volume 54:Issue 9(2015:Sep.) Page Start: 542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗