Found: 22
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Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 710, doi. 10.1002/gcc.23084
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- Publication type:
- Article
Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 10, p. 678, doi. 10.1002/gcc.22977
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- Publication type:
- Article
Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 2, p. 108, doi. 10.1002/gcc.22902
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- Publication type:
- Article
Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 422, doi. 10.1002/gcc.22842
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- Publication type:
- Article
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 567, doi. 10.1002/gcc.22741
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- Publication type:
- Article
Copy number variant analysis using genome‐wide mate‐pair sequencing.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 9, p. 459, doi. 10.1002/gcc.5
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- Publication type:
- Article
Mate‐pair sequencing identifies a cryptic BMPR2 mutation in hereditary pulmonary arterial hypertension.
- Published in:
- Pulmonary Circulation, 2020, v. 10, n. 3, p. 1, doi. 10.1177/2045894020933081
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- Publication type:
- Article
Cover Image.
- Published in:
- 2019
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- Publication type:
- Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
- Published in:
- European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
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- Publication type:
- Article
Shared and unique genomic structural variants of different histological components within testicular germ cell tumours identified with mate pair sequencing.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39956-y
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- Publication type:
- Article
Dual Primary IGH Translocations in Multiple Myeloma: A Novel Finding.
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2021, v. 21, n. 9, p. e710, doi. 10.1016/j.clml.2021.05.001
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- Publication type:
- Article
Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation.
- Published in:
- 2019
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- Publication type:
- journal article
Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2<sup>+</sup> breast cancer samples.
- Published in:
- 2018
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- Publication type:
- journal article
Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia.
- Published in:
- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00908-5
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- Publication type:
- Article
Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma.
- Published in:
- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00851-5
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- Publication type:
- Article
Mass Cytometry reveals unique phenotypic patterns associated with subclonal diversity and outcomes in multiple myeloma.
- Published in:
- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00851-5
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- Publication type:
- Article
Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion.
- Published in:
- Blood Cancer Journal, 2019, v. 9, n. 10, p. N.PAG, doi. 10.1038/s41408-019-0239-z
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- Publication type:
- Article
Novel USP25::PDGFRA Gene Fusion in a 78 Year Old Patient with a Myeloid Neoplasm.
- Published in:
- Laboratory Medicine, 2022, v. 53, n. 5, p. e134, doi. 10.1093/labmed/lmac010
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- Publication type:
- Article
Genome U-Plot: a whole genome visualization.
- Published in:
- Bioinformatics, 2018, v. 34, n. 10, p. 1629, doi. 10.1093/bioinformatics/btx829
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- Publication type:
- Article
Personalized tumor-specific DNA junctions to detect circulating tumor in patients with endometrial cancer.
- Published in:
- PLoS ONE, 2021, v. 16, n. 6, p. 1, doi. 10.1371/journal.pone.0252390
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- Publication type:
- Article
Complex balanced intrachromosomal rearrangement involving PITX2 identified as a cause of Axenfeld‐Rieger Syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 5, p. 1, doi. 10.1002/ajmg.a.63542
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- Publication type:
- Article
Theragnostic chromosomal rearrangements in treatment‐naive pancreatic ductal adenocarcinomas obtained via endoscopic ultrasound.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 8, p. 4110, doi. 10.1111/jcmm.16381
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- Publication type:
- Article