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One or more keywords matched the following items that are connected to Wolff, Daynna
Item TypeName
Academic Article A case of infantile acute myelogenous leukemia with MLL-MLL10 fusion caused by insertion of 11q into 10p.
Academic Article Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities.
Academic Article Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.
Academic Article Altered promoter usage characterizes monoallelic transcription arising with ERBB2 amplification in human breast cancers.
Academic Article Guidance for fluorescence in situ hybridization testing in hematologic disorders.
Academic Article The genetics of bladder cancer: a cytogeneticist's perspective.
Academic Article Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.
Academic Article Mosaic duplication 1(q11q44) in an infant with nephroblastomatosis and mineralization of extraplacental membranes.
Academic Article Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.
Academic Article Jumping translocation of 1q in BCR/ABL-positive acute lymphoblastic leukemia.
Academic Article Laboratory guideline for Turner syndrome.
Academic Article Association of age with fluorescence in situ hybridization abnormalities in multiple myeloma reveals higher rate of IGH translocations among older patients.
Academic Article American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders.
Concept Chromosomes, Human, Pair 16
Concept Chromosome Banding
Concept Chromosomes, Human
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 5
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 13
Academic Article Evaluation of urovysion and cytology for bladder cancer detection: a study of 1835 paired urine samples with clinical and histologic correlation.
Academic Article "Low-Fat" Pseudoangiomatous Spindle Cell Lipoma: A Rare Variant With Loss of 13q14 Region.
Academic Article A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays.
Academic Article Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.
Academic Article Urothelial carcinoma of donor origin in a kidney transplant patient.
Academic Article 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.
Academic Article Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
Academic Article Clinical utility of chromosomal microarray in establishing clonality and high risk features in patients with Richter transformation.
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  • Chromosomes