Found: 8
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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
Quantitative analysis of chromatin interaction changes upon a 4.3 Mb deletion at mouse 4E2.
- Published in:
- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/s12864-015-2137-5
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- Publication type:
- Article
Identical repeated backbone of the humangenome.
- Published in:
- BMC Genomics, 2010, v. 11, p. 60, doi. 10.1186/1471-2164-11-60
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- Publication type:
- Article
Concomitant 1p/19q co-deletion and IDH1/2, ATRX, and TP53 mutations within a single clone of "dual-genotype" IDH-mutant infiltrating gliomas.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1105, doi. 10.1007/s00401-020-02141-x
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- Article
Molecular characterization and reclassification of a 1.18 Mbp DMD duplication following positive carrier screening for Duchenne/Becker muscular dystrophy.
- Published in:
- 2022
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- Publication type:
- Case Study
Prenatal characterization of a novel inverted SMAD2 duplication by mate pair sequencing in a fetus with dextrocardia.
- Published in:
- Clinical Case Reports, 2021, v. 9, n. 2, p. 769, doi. 10.1002/ccr3.3608
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- Publication type:
- Article
Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.1022918
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- Publication type:
- Article
Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 10, p. 1753, doi. 10.1093/hmg/ddz036
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- Publication type:
- Article