Found: 9
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Supravalvular Aortic Stenosis Caused by a Familial Chromosome 7 Inversion Disrupting the ELN Gene Uncovered by Whole-Genome Sequencing.
- Published in:
- Molecular Syndromology, 2019, v. 10, n. 4, p. 209, doi. 10.1159/000500215
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- Publication type:
- Article
BRCA1/BRCA2 germline mutations and chemotherapy-related hematological toxicity in breast cancer patients.
- Published in:
- Breast Cancer Research & Treatment, 2019, v. 174, n. 3, p. 775, doi. 10.1007/s10549-018-05127-2
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- Publication type:
- Article
Compound blue nevus: a reappraisal of the concept in the genomic era.
- Published in:
- 2020
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- Publication type:
- journal article
Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63759-1
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- Publication type:
- Article
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
- Published in:
- BMC Medical Genomics, 2018, v. 11, p. 1, doi. 10.1186/s12920-018-0338-x
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- Publication type:
- Article
Publisher Correction: Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes.
- Published in:
- 2020
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- Publication type:
- Correction Notice
Hyperprogressive Disease After Combined Anti-PD-L1 and Anti-CTLA-4 Immunotherapy for MSI-H/dMMR Gastric Cancer: A Case Report.
- Published in:
- 2021
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- Publication type:
- Case Study
Overview of the Genetic Causes of Hereditary Breast and Ovarian Cancer Syndrome in a Large French Patient Cohort.
- Published in:
- Cancers, 2023, v. 15, n. 13, p. 3420, doi. 10.3390/cancers15133420
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- Publication type:
- Article
Alterations in Homologous Recombination-Related Genes and Distinct Platinum Response in Metastatic Triple-Negative Breast Cancers: A Subgroup Analysis of the ProfiLER-01 Trial.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 10, p. 1595, doi. 10.3390/jpm12101595
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- Publication type:
- Article