Last Updated: 09/26/2026
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Found 15 publications
Genotype-Phenotype Correlations in Klinefelter and Turner Syndrome: A Decade of Sex Chromosome Aneuploidy Data From a Single Academic Medical Center.
Journal: Molecular genetics & genomic medicine
Published: June 23, 2025
A multicenter analysis of individuals with a 47,XXY/46,XX karyotype.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 12, 2024
Evidence-based review of genomic aberrations in diffuse large B cell lymphoma, not otherwise specified (DLBCL, NOS): Report from the cancer genomics consortium lymphoma working group.
Journal: Cancer genetics
Published: May 02, 2022
Artificial Intelligence in Plasma Cell Myeloma: Neural Networks and Support Vector Machines in the Classification of Plasma Cell Myeloma Data at Diagnosis.
Journal: Journal of pathology informatics
Published: April 09, 2021
Clinical diagnosis of neurofibromatosis type I in multiple family members due to cosegregation of a unique balanced translocation with disruption of the NF1 locus: Testing considerations for accurate diagnosis.
Journal: American journal of medical genetics. Part A
Published: June 23, 2020
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.
Journal: Cancer genetics
Published: September 28, 2019
Sustained remission in a patient with PDGFR-beta-rearranged T-lymphoblastic lymphoma and complete remission with dasatinib.
Journal: Pediatric blood & cancer
Published: June 18, 2019
Clinicopathologic correlates of MYD88 L265P mutation and programmed cell death (PD-1) pathway in primary central nervous system lymphoma.
Journal: Leukemia & lymphoma
Published: June 12, 2019
BCR-ABL1-like B-Lymphoblastic Leukemia/Lymphoma with FOXP1-ABL1 Rearrangement: Comprehensive Laboratory Identification Allowing Tyrosine Kinase Inhibitor Use.
Journal: Laboratory medicine
Published: November 10, 2018
Limited Utility of Fluorescence In Situ Hybridization for Recurrent Abnormalities in Acute Myeloid Leukemia at Diagnosis and Follow-up.
Journal: American journal of clinical pathology
Published: March 15, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.
Journal: Cancer genetics
Published: March 11, 2018
Last Updated: 09/26/2026