1. A comprehensive laboratory‐based program for classification of variants of uncertain significance in hereditary cancer genes. (20th December 2013) Authors: Eggington, J.M.; Bowles, K.R.; Moyes, K.; Manley, S.; Esterling, L.; Sizemore, S.; Rosenthal, E.; Theisen, A.; Saam, J.; Arnell, C.; Pruss, D.; Bennett, J.; Burbidge, L.A.; Roa, B.; Wenstrup, R.J. Journal: Clinical genetics Issue: Volume 86:Number 3(2014:Sep.) Page Start: 229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of current testing practices for biallelic MUTYH mutations in MUTYH‐associated polyposis. (10th May 2014) Authors: Landon, M.; Ceulemans, S.; Saraiya, D.S.; Strike, B.; Arnell, C.; Burbidge, L.A.; Moyes, K.; Theisen, A.; Fernandes, P.H.; Ji, J.Q.; Abbott, B.; Kaldate, R.R.; Roa, B. Journal: Clinical genetics Issue: Volume 87:Number 4(2015:Apr.) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗