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Molecular Cytogenetics|August 11, 2015
Observations of the genomic landscape beyond 1p19q deletions and EGFR amplification in gliomaChristian N Paxton, Leslie R Rowe, Sarah T SouthJournal of the Association of Genetic Technologists|July 28, 2015
Streamlining the OncoScan® Array Procedure for Use in a Clinical LaboratoryChristian N Paxton, Leslie R Rowe, Sarah T SouthPediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|June 20, 2014
Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by genomic microarray analysisIsaac E Lloyd, Leslie R Rowe, Lance K Erickson, et al.American Journal of Clinical Pathology|June 12, 2016
Two Unrelated Burkitt Lymphomas Seven Years Apart in a Patient With X-Linked Lymphoproliferative Disease Type 1 (XLP1)Delu Zhou, Christian N Paxton, Todd W Kelley, et al.American Journal of Medical Genetics. Part A|November 23, 2011
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disabilityAlison Millson, Danielle Lagrave, Mary J H Willis, et al.American Journal of Medical Genetics. Part A|August 24, 2016
Braddock-Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1Stephen R Braddock, Sarah T South, Joshua D Schiffman, et al.Archives of Pathology & Laboratory Medicine|August 2, 2012
Differentiation of malignant melanoma from benign nevus using a novel genomic microarray with low specimen requirementsWells M Chandler, Leslie R Rowe, Scott R Florell, et al.The Journal of Molecular Diagnostics : JMD|May 14, 2013
Molecular inversion probe array for the genetic evaluation of stillbirth using formalin-fixed, paraffin-embedded tissueLeslie R Rowe, Harshwardhan M Thaker, John M Opitz, et al.Clinics in Laboratory Medicine|November 29, 2011
Chromosomal structural rearrangements: detection and elucidation of mechanisms using cytogenomic technologiesSarah T SouthModern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 29, 2017
Genetic evaluation of juvenile xanthogranuloma: genomic abnormalities are uncommon in solitary lesions, advanced cases may show more complexityChristian N Paxton, Dennis P O'Malley, Andrew M Bellizzi, et al.Pageof 10