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Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 12, 2014
Masked hypodiploidy in anaplastic meningiomas by duplication of the original clone found in atypical meningiomas: illustration of the evolution of genetic alterationsErin E Ely, Miguel A Guzman, Laura S Calvey, et al.Journal of Pediatric Hematology/Oncology|September 30, 2004
Lymphoblastic leukemia with mature B-cell phenotype in infancyJohn L Frater, Jacqueline R Batanian, Dennis M O'Connor, et al.Case Reports in Oncology|December 19, 2014
Papillary thyroid cancer in struma testis with malignant transformation in the lung associated with trisomy 17 successfully treated with total thyroidectomy and radioiodine ablationShadi Barakat, Jamie Odem, Jacqueline R Batanian, et al.Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 5, 2018
Novel TLE4-NTRK2 fusion in a ganglioglioma identified by array-CGH and confirmed by NGS: Potential for a gene targeted therapyNitya Prabhakaran, Miguel A Guzman, Pournima Navalkele, et al.Cancer Genetics|September 18, 2013
Narrowing down the common deleted region of 5q to 6.0 Mb in blastic plasmacytoid dendritic cell neoplasmsYumei Fu, Mark Fesler, Gibran Mahmud, et al.Cancer Genetics and Cytogenetics|March 14, 2002
EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22)Jacqueline R Batanian, Julia A Bridge, Robert Wickert, et al.Pediatric Neurology|April 29, 2014
Malignant transformation of a desmoplastic infantile ganglioglioma in an infant carrier of a nonsynonymous TP53 mutationVikram Prakash, Jacqueline R Batanian, Miguel A Guzman, et al.Cancer Genetics|August 29, 2015
Cryptic insertion of 3'FOXO1 into inverted chromosome arm 2q in the presence of two normal chromosome 13s and 13 small interstitial duplications in a patient with alveolar rhabdomyosarcomaSarah Hackman, Laura Calvey, Kristen Bernreuter, et al.American Journal of Medical Genetics. Part A|March 26, 2014
An intragenic deletion of the gene MNAT1 in a family with pectus deformitiesJennifer L Heithaus, Sandra Davenport, Kimberly A Twyman, et al.Journal of Cutaneous Pathology|June 11, 2020
A novel aberration of COL1A1-PDGFB fusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare locationAlexander Daoud, Christopher R Cunningham, Jessica A Kozel, et al.Pageof 4