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The British Journal of Ophthalmology|January 8, 2013
Molecular testing prognostic of low risk in epithelioid uveal melanoma in a childHelen Dimaras, Manoj Vijay Parulekar, Grace Kwok, et al.American Journal of Medical Genetics. Part A|July 9, 2011
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)David L Skidmore, David Chitayat, Tim Morgan, et al.CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 29, 2003
West Nile virus infection in 2002: morbidity and mortality among patients admitted to hospital in southcentral OntarioCaitlin Pepperell, Neil Rau, Sigmund Krajden, et al.Human Molecular Genetics|January 30, 2013
Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndromeKaren Buysse, Moniek Riemersma, Gareth Powell, et al.The Lancet. Oncology|March 19, 2013
Characterisation of retinoblastomas without RB1 mutations: genomic, gene expression, and clinical studiesDiane E Rushlow, Berber M Mol, Jennifer Y Kennett, et al.Acta Neuropathologica|May 21, 2014
CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entityTara Spence, Patrick Sin-Chan, Daniel Picard, et al.Pageof 5