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A case of infantile acute myelogenous leukemia with MLL-MLL10 fusion caused by insertion of 11q into 10p.
Abnormal fluorescence in situ hybridization analysis in collecting duct carcinoma.
Fluorescence in situ hybridization for detecting transitional cell carcinoma: implications for clinical practice.
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.
HER2 testing: a review of detection methodologies and their clinical performance.
Guidance for fluorescence in situ hybridization testing in hematologic disorders.
The genetics of bladder cancer: a cytogeneticist's perspective.
Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.
The utility of fluorescence in situ hybridization (FISH) analysis in diagnosing graft versus host disease following orthotopic liver transplant.
Validation of fluorescence in situ hybridization using an analyte-specific reagent for detection of abnormalities involving the mixed lineage leukemia gene.
HER-2 fluorescence in situ hybridization: results from the survey program of the College of American Pathologists.
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia.
Association of age with fluorescence in situ hybridization abnormalities in multiple myeloma reveals higher rate of IGH translocations among older patients.
In Situ Hybridization, Fluorescence
Evaluation of urovysion and cytology for bladder cancer detection: a study of 1835 paired urine samples with clinical and histologic correlation.
"Low-Fat" Pseudoangiomatous Spindle Cell Lipoma: A Rare Variant With Loss of 13q14 Region.
A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays.
Comparison Between HER2, Estrogen Receptors and Progesterone Receptors in Primary Breast Carcinomas and Matched Lymph Node Metastases.
Urothelial carcinoma of donor origin in a kidney transplant patient.
Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia.
Novel high-risk acute myeloid leukemia subgroup with ERG amplification and Biallelic loss of TP53.