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Clinicopathologic and Molecular Characteristics of Resected Thoracic Mass Lesions in the Pediatric Population: A 25-Year Institutional Experience From a Tertiary Care Center.
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- Archives of Pathology & Laboratory Medicine, 2024, v. 148, n. 11, p. 1209, doi. 10.5858/arpa.2023-0251-OA
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- Article
Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia.
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- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00908-5
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- Article
Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.
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- Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 710, doi. 10.1002/gcc.23084
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- Article
Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
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- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 422, doi. 10.1002/gcc.22842
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- Article
RNA sequencing identifies a novel USP9X‐USP6 promoter swap gene fusion in a primary aneurysmal bone cyst.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 589, doi. 10.1002/gcc.22742
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- Article
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 567, doi. 10.1002/gcc.22741
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- Article
Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal Neoplasia.
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- JAMA Network Open, 2021, v. 4, n. 11, p. e2132615, doi. 10.1001/jamanetworkopen.2021.32615
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- Article
Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis.
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- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0455-z
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- Article
Cover Image.
- Published in:
- 2019
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- Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
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- European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
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- Article
Mate pair sequencing outperforms fluorescence in situ hybridization and improves diagnostic yield in the genomic characterization of multiple myeloma.
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- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. e58, doi. 10.1016/j.clml.2019.09.090
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- Article
Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma.
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- Blood Cancer Journal, 2019, v. 9, n. 12, p. 1, doi. 10.1038/s41408-019-0255-z
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- Article
Clinical utility of fluorescence in situ hybridization‐based diagnosis of BCR‐ABL1 like (Philadelphia chromosome like) B‐acute lymphoblastic leukemia.
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- American Journal of Hematology, 2020, v. 95, n. 3, p. E68, doi. 10.1002/ajh.25729
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- Article
A TRIP11:: FLT3 gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature.
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- Cold Spring Harbor Molecular Case Studies, 2023, v. 9, n. 1, p. 1, doi. 10.1101/mcs.a006243
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- Article
Molecular and Immunophenotypic Correlates of Metastatic Epithelioid Angiomyolipoma Include Alterations of TP53, RB1, and ATRX.
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- Archives of Pathology & Laboratory Medicine, 2023, v. 147, n. 7, p. 817, doi. 10.5858/arpa.2022-0127-OA
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- Article