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	Title	Author(s)	Issue Date
	Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice Journal:Journal of Medical Genetics	Bruno, DL Ganesamoorthy, D Schoumans, J Bankier, A Coman, D Delatycki, M Gardner, RJM Hunter, M James, PA Kannu, P Mcgillivray, G Pachter, N Peters, H Rieubland, C Savarirayan, R Scheffer, IE Sheffield, L Tan, T White, SM Yeung, A Bowman, Z Ngo, C Choy, KW Cacheux, V Wong, L Amor, DJ Slater, HR	2009
	SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals Journal:Human Mutation	Ng, BG Sosicka, P Agada, S Almannai, M Bacino, CA Barone, R Botto, L Burton, JE Carlston, C Chung, BHY Cohen, J Coman, D Dobyns, W Elias, AF Epstein, L Garozzo, D Grunewald, S Hammer, TB Haven, J Heron, D Hoganson, GE Lakhani, S Lee, J Lewis, K Longo, N Lourenco, CM Mak, CCY Mendelsohn, B Mignnot, C Mirzaa, G Mitchell, W Olezak, M Parikian, A Patterson, MC Pierson, T Quinonez, SC Regan, B Rosa, ME Scaglia, F Scheffer, I Segal, D Singhal, NS Striano, P Sturiale, L Symonds, J Willis, M Wolfe, LA Yano, S Powis, Z Suchy, S Mokry, JA Edmondson, AC Freeze, HH	2019

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