V. Hastings

Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group.

L. Surh, M. Cappelli, A. Hunter, 1995, American journal of human genetics.

Severe craniosynostosis in an infant with deletion 22q11.2 syndrome

J. McGowan-Jordan, W. Al-Hertani, G. Graham, 2013, American journal of medical genetics. Part A.

Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma.

S. Bens, R. Siebert, A. Mes-Masson, 2017, Cancer research.

Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada

W. Foulkes, N. Hamel, T. Hartley, 2014, Hereditary cancer in clinical practice.

Feasibility Study and Clinical Impact of Incorporating Breast Tissue Density in High-Risk Breast Cancer Screening Assessment

J. Seely, E. Tomiak, Caitlin E Aldridge, 2022, Current oncology.