Found: 13
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Relationship between FRA11F and 11q13 gene amplification in oral cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 2, p. 143, doi. 10.1002/gcc.20394
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- Publication type:
- Article
Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2022, v. 8, n. 2, p. 1, doi. 10.1101/mcs.a006180
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- Publication type:
- Article
Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2020, v. 6, n. 3, p. 1, doi. 10.1101/mcs.a005231
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- Article
Mapping and analysis of HPV16 integration sites in a head and neck cancer cell line.
- Published in:
- International Journal of Cancer, 2004, v. 110, n. 5, p. 701, doi. 10.1002/ijc.20193
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- Publication type:
- Article
Genomic analyses identify recurrent MEF2D fusions in acute lymphoblastic leukaemia.
- Published in:
- Nature Communications, 2016, v. 7, n. 11, p. 13331, doi. 10.1038/ncomms13331
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- Article
5′ ALK Amplification in Neuroblastoma: A Case Report.
- Published in:
- Case Reports in Oncology, 2021, v. 14, n. 1, p. 585, doi. 10.1159/000512187
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- Publication type:
- Article
Chromosomal instability and marker chromosome evolution in oral squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 1, p. 38, doi. 10.1002/gcc.20064
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- Publication type:
- Article
Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 1997, v. 20, n. 2, p. 185, doi. 10.1002/(SICI)1098-2264(199710)20:2<185::AID-GCC9>3.0.CO;2-#
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- Publication type:
- Article
Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.
- Published in:
- Pediatric Cardiology, 2019, v. 40, n. 8, p. 1679, doi. 10.1007/s00246-019-02203-2
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- Article
Immune Reconstitution after Hematopoietic Stem Cell Transplantation in Immunodeficiency–Centromeric Instability–Facial Anomalies Syndrome Type 1.
- Published in:
- 2021
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- Publication type:
- Letter
Expanding the Clinical Utility of Targeted RNA Sequencing Panels beyond Gene Fusions to Complex, Intragenic Structural Rearrangements.
- Published in:
- Cancers, 2023, v. 15, n. 17, p. 4394, doi. 10.3390/cancers15174394
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- Publication type:
- Article
Microarray comparative genomic hybridization and cytogenetic characterization of tissue-specific mosaicism in three patients.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 1924, doi. 10.1002/ajmg.a.35477
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- Publication type:
- Article
Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.
- Published in:
- Cytogenetic & Genome Research, 2017, v. 152, n. 2, p. 105, doi. 10.1159/000478921
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- Publication type:
- Article