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
Pediatric fibromyxoid soft tissue tumor with PLAG1 fusion: A novel entity?
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 4, p. 263, doi. 10.1002/gcc.22926
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- Publication type:
- Article
Genetic diversity in alveolar soft part sarcoma: A subset contain variant fusion genes, highlighting broader molecular kinship with other MiT family tumors.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 1, p. 23, doi. 10.1002/gcc.22803
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- Publication type:
- Article
TFE3-Expressing Perivascular Epithelioid Cell Neoplasm (PEComa) of the Sella Turcica.
- Published in:
- Endocrine Pathology, 2017, v. 28, n. 1, p. 22, doi. 10.1007/s12022-016-9434-7
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- Article
Favorable survival and metabolic outcome for children with diencephalic syndrome using a radiation-sparing approach.
- Published in:
- Journal of Neuro-Oncology, 2014, v. 116, n. 1, p. 195, doi. 10.1007/s11060-013-1284-2
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- Publication type:
- Article
Cryptic insertion of MLL gene into 9p22 leads to MLL–MLLT3 (AF9) fusion in a case of acute myelogenous leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 40, n. 4, p. 349, doi. 10.1002/gcc.20045
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- Publication type:
- Article
Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories.
- Published in:
- 2021
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- Publication type:
- journal article
Cribriform neuroepithelial tumour: novel clinicopathological, ultrastructural and cytogenetic findings.
- Published in:
- 2011
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- Publication type:
- Letter
Myeloproliferative Neoplasm Driven by ETV6-ABL1 in an Adolescent with Recent History of Burkitt Leukemia.
- Published in:
- Current Oncology, 2023, v. 30, n. 7, p. 5946, doi. 10.3390/curroncol30070444
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- Publication type:
- Article
Genome assembly comparison identifies structural variants in the human genome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 12, p. 1413, doi. 10.1038/ng1921
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- Publication type:
- Article
TERT promotor variant associated with poor clinical outcome in a patient with novel RBM15‐MKL1 fusion‐positive pediatric acute megakaryoblastic leukemia.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 1, p. 1, doi. 10.1002/pbc.28542
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- Publication type:
- Article
Frequency and outcome of pediatric acute lymphoblastic leukemia with ZNF384 gene rearrangements including a novel translocation resulting in an ARID1B/ZNF384 gene fusion.
- Published in:
- 2016
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- Publication type:
- journal article
The Diploid Genome Sequence of an Individual Human.
- Published in:
- PLoS Biology, 2007, v. 5, n. 10, p. e254, doi. 10.1371/journal.pbio.0050254
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- Publication type:
- Article
Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.
- Published in:
- Scientific Reports, 2016, p. 28663, doi. 10.1038/srep28663
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- Publication type:
- Article
An aggressive central giant cell granuloma in a pediatric patient: case report and review of literature.
- Published in:
- Journal of Otolaryngology -- Head & Neck Surgery, 2019, v. 48, n. 1, p. N.PAG, doi. 10.1186/s40463-019-0356-5
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- Publication type:
- Article
Splenic hamartoma in a child in the era of PET-CT.
- Published in:
- Pediatric Blood & Cancer, 2009, v. 53, n. 1, p. 114, doi. 10.1002/pbc.21962
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- Publication type:
- Article
Toxicity and outcome of children with treatment related acute myeloid leukemia.
- Published in:
- Pediatric Blood & Cancer, 2008, v. 50, n. 1, p. 17, doi. 10.1002/pbc.21157
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- Publication type:
- Article
TEL-AML1 fusion in acute lymphoblastic leukemia with L3 morphology.
- Published in:
- Pediatric Blood & Cancer, 2007, v. 49, n. 2, p. 217, doi. 10.1002/pbc.20962
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- Publication type:
- Article
45,X/46,XY mosaicism: Clinical manifestations and long term follow‐up.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 3, p. 1, doi. 10.1002/ajmg.a.63451
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- Publication type:
- Article
Mosaic microdeletion of 17p11.2-p12 and duplication of 17q22-q24 in a girl with Smith-Magenis phenotype and peripheral neuropathy.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 748, doi. 10.1002/ajmg.a.36322
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- Publication type:
- Article
SMARCAL1 deficiency predisposes to non-Hodgkin lymphoma and hypersensitivity to genotoxic agents in vivo.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2204, doi. 10.1002/ajmg.a.35532
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- Publication type:
- Article
Definition of a critical genetic interval related to kidney abnormalities in the Potocki-Lupski syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1579, doi. 10.1002/ajmg.a.35399
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- Publication type:
- Article