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Canadian Journal of Gastroenterology & Hepatology|November 30, 2013
Follow-up of participants in the Canadian Association of Gastroenterology Scholars' Program, 2006 to 2012Mindy Ching Wan Lam, Michael Sl Sey, Jamie Gregor, et al.Journal of Visualized Experiments : Jove|January 17, 2014
Laser-scanning photostimulation of optogenetically targeted forebrain circuitsCharles C Lee, Ying-Wan Lam, Kazuo Imaizumi, et al.International Journal of Oncology|May 24, 2008
Genomic analyses identify gene candidates for acquired irinotecan resistance in melanoma cellsKai Gao, William W Lockwood, Jun Li, et al.Journal of Paediatrics and Child Health|October 22, 2008
Hyperinsulinism and hyperammonaemia syndrome due to a novel missense mutation in the allosteric domain of the glutamate dehydrogenase 1 geneKar-Ki Chik, Chun-Wing Chan, Ching-Wan Lam, et al.Rapid Communications in Mass Spectrometry : RCM|December 17, 2011
Organochlorine isotopic pattern-enhanced detection and quantification of triclosan and its metabolites in human serum by ultra-high-performance liquid chromatography/quadrupole time-of-flight/mass spectrometryJian-lin Wu, Ka-Fai Leung, Sui-Fan Tong, et al.Biological Procedures Online|October 22, 2003
Two-dimensional DNA displays for comparisons of bacterial genomesChad Malloff, Edie Dullaghan, Alice Li, et al.Journal of Cardiovascular Electrophysiology|January 13, 2006
Ketoconazole induced torsades de pointes without concomitant use of QT interval-prolonging drugNgai-Shing Mok, Ying-Keung Lo, Ping-Tim Tsui, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 24, 2013
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivationSun Young Cho, Ching-wan Lam, Sui-Fan Tong, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|February 2, 2016
Novel large deletion in AVPR2 gene causing copy number variation in a patient with X-linked nephrogenic diabetes insipidusSun Young Cho, Chun Yiu Law, Kwok Leung Ng, et al.European Journal of Human Genetics : EJHG|December 15, 2016
Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutationsChing-Wan Lam, Ka-Sing Wong, Ho-Wan Leung, et al.Pageof 21