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Genome Biology|June 23, 2007
Genome position and gene amplificationPavla Gajduskova, Antoine M Snijders, Serena Kwek, et al.Advances in Chronic Kidney Disease|March 13, 2008
Geriatric hemodialysis rehabilitation careSarbjit Vanita Jassal, Ernest Chiu, Marilyn LiOncogene|April 13, 2005
Rare amplicons implicate frequent deregulation of cell fate specification pathways in oral squamous cell carcinomaAntoine M Snijders, Brian L Schmidt, Jane Fridlyand, et al.Genes, Chromosomes & Cancer|October 18, 2006
Chromosomal aberrations in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma unspecified: A matrix-based CGH approachChristoph Thorns, Boris Bastian, Daniel Pinkel, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 20, 2005
Array comparative genomic hybridization identifies genetic subgroups in grade 4 human astrocytomaAnjan Misra, Malgorzata Pellarin, Janice Nigro, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 27, 2007
Quality improvement through the introduction of interdisciplinary geriatric hemodialysis rehabilitation careMarilyn Li, Eveline Porter, Robert Lam, et al.Journal of Clinical Anesthesia|September 2, 2008
Paradoxical postural cerebrospinal fluid leak-induced headache: report of two casesHenry Liu, Alan D Kaye, Neal Comarda, et al.Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|December 30, 2004
Genomic alterations in primary gastric adenocarcinomas correlate with clinicopathological characteristics and survivalMarjan M Weiss, Ernst J Kuipers, Cindy Postma, et al.American Journal of Medical Genetics. Part A|October 4, 2005
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridizationOphir D Klein, Philip D Cotter, Ann M Schmidt, et al.American Journal of Medical Genetics. Part A|March 31, 2007
Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model systemTaku A Tokuyasu, Philip D Cotter, Richard Segraves, et al.Pageof 11