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SLC22A4 Gene in Hereditary Non-syndromic Hearing Loss: Recurrence and Incomplete Penetrance of the p.C113Y Mutation in Northwest Africa.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.606630
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- Article
Clonal dynamics and copy number variants by single‐cell analysis in leukemic evolution of myeloproliferative neoplasms.
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- American Journal of Hematology, 2023, v. 98, n. 10, p. 1520, doi. 10.1002/ajh.27013
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- Article
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer.
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- Cancers, 2023, v. 15, n. 10, p. 2666, doi. 10.3390/cancers15102666
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- Article
Post-Biopsy Cell-Free DNA From Blood: An Open Window on Primary Prostate Cancer Genetics and Biology.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.654140
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- Article
Mutated clones driving leukemic transformation are already detectable at the single-cell level in CD34-positive cells in the chronic phase of primary myelofibrosis.
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- NPJ Precision Oncology, 2021, v. 5, n. 1, p. 1, doi. 10.1038/s41698-021-00144-9
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- Article
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss.
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- Cells (2073-4409), 2022, v. 11, n. 11, p. 1726, doi. 10.3390/cells11111726
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- Article
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear.
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- PLoS ONE, 2023, v. 17, n. 1, p. 1, doi. 10.1371/journal.pone.0273586
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- Article
The Genetics of Myelodysplastic Syndromes: Clinical Relevance.
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- Genes, 2021, v. 12, n. 8, p. 1144, doi. 10.3390/genes12081144
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- Article
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178630
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- Article