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Hebert, Robyn; Cullinan, Noelle; Armstrong, Linlea; Blood, Katherine A; Brossard, Josee; Brunga, Ledia; Cacciotti, Chantel; Caswell, Kimberly; Cellot, Sonia; Coltin, Hallie; Deyell, Rebecca J; Felton, Kathleen; Fernandez, Conrad V; Fleming, Adam J; Gibson, Paul; Hammad, Rawan; Jabado, Nada; Johnston, Donna L; Lafay-Cousin, Lucie; Larouche, Valérie; ... (2023). Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes. Journal of medical genetics, 60(12), pp. 1218-1223. BMJ Publishing Group 10.1136/jmg-2023-109376
Goudie, Catherine; Witkowski, Leora; Cullinan, Noelle; Reichman, Lara; Schiller, Ian; Tachdjian, Melissa; Armstrong, Linlea; Blood, Katherine A; Brossard, Josée; Brunga, Ledia; Cacciotti, Chantel; Caswell, Kimberly; Cellot, Sonia; Clark, Mary Egan; Clinton, Catherine; Coltin, Hallie; Felton, Kathleen; Fernandez, Conrad V; Fleming, Adam J; Fuentes-Bolanos, Noemi; ... (2021). Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes. JAMA oncology, 7(12), pp. 1806-1814. American Medical Association 10.1001/jamaoncol.2021.4536
Renzi, Samuele; Langenberg-Ververgaert, Karin Petra Sabine; Waespe, Nicolas; Ali, Salah; Bartram, Jack; Michaeli, Orli; Upton, Julia; Cada, Michaela (2020). Primary immunodeficiencies and their associated risk of malignancies in children: an overview. European journal of pediatrics, 179(5), pp. 689-697. Springer-Verlag 10.1007/s00431-020-03619-2
