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JAAPA : Official Journal of the American Academy of Physician Assistants|February 6, 2018
Postpartum depression in older womenBrittany Strelow, Nicole Fellows, Stephanie R Fink, et al.The American Journal of Surgical Pathology|November 24, 2006
The incidence and anatomic site specificity of chromosomal translocations in primary extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) in North AmericaEllen D Remstein, Ahmet Dogan, Richard R Einerson, et al.Leukemia Research|January 3, 2009
Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocationsStephanie R Fink, Kimberly J Belongie, Sarah F Paternoster, et al.Cancer Genetics and Cytogenetics|February 27, 2007
Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20qStephanie A Smoley, Stephanie R Fink, Sarah F Paternoster, et al.Leukemia Research|November 28, 2006
Efficacy of conventional cytogenetics and FISH for EGR1 to detect deletion 5q in hematological disorders and to assess response to treatment with LenalidomideYing S Zou, Stephanie R Fink, Kimberly J Stockero, et al.Leukemia Research|January 22, 2005
Fluorescent-labeled DNA probes applied to novel biological aspects of B-cell chronic lymphocytic leukemiaStephanie R Fink, Sarah F Paternoster, Stephanie A Smoley, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2006
Preclinical validation of fluorescence in situ hybridization assays for clinical practiceAnne E Wiktor, Daniel L Van Dyke, Peggy J Stupca, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 8, 2011
MYC gene amplification is often acquired in lethal distant breast cancer metastases of unamplified primary tumorsAatur D Singhi, Ashley Cimino-Mathews, Robert B Jenkins, et al.Cancer Genetics and Cytogenetics|April 25, 2006
Metaphase cells with normal G-bands have cryptic interstitial deletions in 13q14 detectable by fluorescence in situ hybridization in B-cell chronic lymphocytic leukemiaKimberly J Stockero, Stephanie R Fink, Stephanie A Smoley, et al.Cancer Genetics and Cytogenetics|June 2, 2006
Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemiaStephanie R Fink, Stephanie A Smoley, Kimberly J Stockero, et al.Pageof 2