I. Ambus

BRCA1/2 predictive testing: a study of uptake in two centres

R. Eeles, A. Ardern-Jones, D. Craufurd, 2004, European Journal of Human Genetics.

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

R. Weksberg, J. Squire, P. Ray, 2001, Human molecular genetics.

IDH1 mutated low grade astrocytoma occurring in MSH2 mutated Lynch syndrome family

C. Rowsell, L. Velsher, J. Keith, 2016 .

The importance of functional testing in the genetic assessment of Muir-Torre syndrome, a clinical subphenotype of HNPCC.

P. Peltomäki, H. Lynch, T. Raevaara, 2006, International journal of oncology.

Pilot Testing of a Psycho-educational Telephone Intervention for Women Receiving Uninformative BRCA1/2 Genetic Test Results.

W. Meschino, J. Honeyford, C. Maheu, 2015, The Canadian journal of nursing research = Revue canadienne de recherche en sciences infirmieres.

Germline variants and phenotypic spectrum in a Canadian cohort of individuals with diffuse gastric cancer.

Z. Cohen, W. Meschino, A. Govindarajan, 2019, Current oncology.