Marie L. Dell'aquila
Medical Genetics
9500 Gilman Dr
Ucsd Division Of Medical Genetics-0639
La Jolla, CA 92093
Ucsd Division Of Medical Genetics-0639
La Jolla, CA 92093
Last Updated: 09/26/2026
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Found 12 publications
A CD10-negative adult B-lymphoblastic leukaemia with amplification of KMT2A without rearrangement: A case report and review of the English literature.
Journal: British journal of haematology
Published: March 07, 2024
Acute myeloid leukaemia evolving from essential thrombocythaemia with marked KMT2A amplification as a homogenously staining region.
Journal: British journal of haematology
Published: May 28, 2019
Implementation of the 2018 American Society of Clinical Oncology/College of American Pathologists Guidelines on HER2/neu Assessment by FISH in breast cancers: predicted impact in a single institutional cohort.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: February 26, 2019
JAK2 double minutes with resultant simultaneous amplification of JAK2 and CD274 in a therapy-related myelodysplastic syndrome evolving into an acute myeloid leukaemia.
Journal: British journal of haematology
Published: August 23, 2018
Comparative Pathologic Analysis of Breast Cancers Classified as HER2/neu-Amplified by FISH Using a Standard HER2/CEP17 Dual Probe and an Alternative Chromosome 17 Control Probe.
Journal: The American journal of surgical pathology
Published: June 21, 2018
Her2/neu Status Determination in Breast Cancer: A Single Institutional Experience Using a Dual-Testing Approach With Immunohistochemistry and Fluorescence In Situ Hybridization.
Journal: American journal of clinical pathology
Published: March 25, 2017
Successful treatment of both double minute of C-MYC and BCL-2 rearrangement containing large B-cell lymphoma with subsequent unfortunate development of therapy-related acute myeloid leukemia with t(3;3)(q26.2;q21).
Journal: Pathology, research and practice
Published: May 25, 2015
Nodal involvement by marginal zone B-cell lymphoma harboring t(14;22)(q32;q11) involving immunoglobulin heavy chain and light chain lambda as the sole karyotypically recognizable abnormality in a patient with systemic lupus erythematosus.
Journal: International journal of clinical and experimental pathology
Published: June 10, 2014
Translocation t(2;11) in CLL cells results in CXCR4/MAML2 fusion oncogene.
Journal: Blood
Published: May 24, 2014
Myeloid neoplasm with t(3;8)(q26;q24): report of six cases and review of the literature.
Journal: Leukemia & lymphoma
Published: January 09, 2014
Subclonal evolution involving SF3B1 mutations in chronic lymphocytic leukemia.
Journal: Leukemia
Published: January 23, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026