Related Experiment Videos
A case of myxoid liposarcoma with translocation t(12;16) as the only abnormality
T A Walter1, H J Decker, S P Leong
1Cancer Center, Southwest Biomedical Research Institute, Scottsdale, AZ 85251.
Cancer Genetics and Cytogenetics
|August 1, 1988
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Cytogenetic and fluorescence in situ hybridization analysis of breast fibroadenomas.
Cancer genetics and cytogenetics·1992
Application of fluorescence in situ hybridization in hematological disorders.
Cancer genetics and cytogenetics·1992
Cytogenetic and molecular studies of a familial renal cell carcinoma.
Cancer genetics and cytogenetics·1992
Isolation of a yeast artificial chromosome clone that spans the (12;16) translocation breakpoint characteristic of myxoid liposarcoma.
Cancer genetics and cytogenetics·1992
Cytogenetic and FISH studies of abnormal X chromosomes in a patient with ANLL.
Cancer genetics and cytogenetics·1992
A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.
Cancer genetics and cytogenetics·2010
Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.
Cancer genetics and cytogenetics·2010
Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.
Cancer genetics and cytogenetics·2010
Screening for common copy-number variants in cancer genes.
Cancer genetics and cytogenetics·2010
Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.
Cancer genetics and cytogenetics·2010
Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.
Cancer genetics and cytogenetics·2010
177Lu-FAPI-2286 Radioligand Therapy in Refractory Scalp Melanoma.
Clinical nuclear medicine·2026
Tandem Double Inversion Resolves the Structural Paradox Underlying Recurrent KAT6A::NCOA2 Fusion in Acute Myeloid Leukemia.
Genes, chromosomes & cancer·2026
A novel variant of Type I Abernethy syndrome: branchless intraparenchymal portal vein trunk draining into the right atrium in a 7-year-old girl: a case report and literature review.
International journal of surgery case reports·2026