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Journal of the Association of Genetic Technologists|December 14, 2019
Molecular Cytogenetic Characterization of a Three-way t(8;14;22)(q24;q32;q11.2) with Involvement of MYC/IGH/IGL in a Case of a Diffuse Large B-cell Lymphoma (DLBCL)Carlos A Tirado, Karen Cunnien, Katie Lapp, et al.Journal of the Association of Genetic Technologists|December 14, 2019
A Comprehensive Review of Chronic Myeloid Leukemia: An Indian PerspectivePriya K Varma, Dharmesh M Patel, Pina J Trivedi, et al.Journal of the Association of Genetic Technologists|December 14, 2019
Molecular Cytogenetic Characterization of a Karyotype of a Female Patient with Secondary Amenorrhea with a Cell Line Showing 46,X,+marA Okabe, A Reyes, M Murphy, et al.Journal of the Association of Genetic Technologists|December 14, 2019
The Ups and Downs When TLX-1 and Other Transcriptional Modulators Abound: A Case of T-ALL with a Transcriptionally Complex Set of MutationsLiam Donnelly, Katherine Devitt, Juli-Anne GardnerJournal of the Association of Genetic Technologists|March 19, 2018
Renal Cell Carcinoma with monosomy 8: A Case Series and Review of the LiteratureJustin Rueckert, Katherine Devitt, Juli-Anne GardnerJournal of the Association of Genetic Technologists|June 2, 2015
c-MYC Amplification in Acute Myelogenous Leukemia Evolving from Double Minutes (dmins) to Homogeneously Staining Region (hsr)Farzaneh Sayedian, Jamie R Senft, Michelle D Spruill, et al.Journal of the Association of Genetic Technologists|June 2, 2015
ALK FISH Assays for Non-small Cell Lung Cancer Treatment Selection: Scoring Issues and Probe DesignHelen J Lawce, Susan OlsonJournal of the Association of Genetic Technologists|June 2, 2015
A Cryptic t(11;14) Translocation in Mantle Cell Lymphoma Highlights the Importance of FISHMichael E Kallen, Yeun Kim, Lynn Yang, et al.Journal of the Association of Genetic Technologists|June 2, 2015
Genes, chromosomes, and disorders of sex development: an updateDavid Shabsovich, Carlos A TiradoJournal of the Association of Genetic Technologists|June 2, 2015
Seizure Disorder in a Patient with a 5.09 Mb 7q11.23-q21.11 Microdeletion Including the MAGI2 GeneJess F Peterson, Pankaj Thakur, Abigail Peffer, et al.Pageof 21