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Single-cell transcriptomics and epigenomics unravel the role of monocytes in neuroblastoma bone marrow metastasis.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39210-0
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- Publication type:
- Article
Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36606-w
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- Publication type:
- Article
The impact of chemo- and radiotherapy treatments on selfish de novo FGFR2 mutations in sperm of cancer survivors.
- Published in:
- 2019
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- Publication type:
- journal article
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 15, p. 4015, doi. 10.1093/hmg/ddu115
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- Publication type:
- Article
Comparison of three different methods to detect bone marrow involvement in patients with neuroblastoma.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2022, v. 148, n. 10, p. 2581, doi. 10.1007/s00432-021-03780-7
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- Publication type:
- Article
amplimap: a versatile tool to process and analyze targeted NGS data.
- Published in:
- Bioinformatics, 2020, v. 36, n. 8, p. 2643, doi. 10.1093/bioinformatics/btz905
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- Publication type:
- Article
amplimap: a versatile tool to process and analyze targeted NGS data.
- Published in:
- Bioinformatics, 2019, v. 35, n. 24, p. 5349, doi. 10.1093/bioinformatics/btz582
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- Publication type:
- Article
Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23445-w
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- Publication type:
- Article
Landscape of Bone Marrow Metastasis in Human Neuroblastoma Unraveled by Transcriptomics and Deep Multiplex Imaging.
- Published in:
- Cancers, 2021, v. 13, n. 17, p. 4311, doi. 10.3390/cancers13174311
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- Publication type:
- Article
Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic mosaicism cases.
- Published in:
- Human Mutation, 2017, v. 38, n. 10, p. 1360, doi. 10.1002/humu.23281
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- Publication type:
- Article
Novel Insights into Diagnosis, Biology, and Treatment of Primary Diffuse Leptomeningeal Melanomatosis.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 4, p. 292, doi. 10.3390/jpm11040292
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- Publication type:
- Article