Found: 4
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An endothelial growth factor receptor compound mutation of T790M substitution with exon 19 deletion in a previously untreated patient: a case report.
- Published in:
- 2019
- By:
- Publication type:
- journal article
A Novel APOC2 Mutation in a Colombian Patient with Recurrent Hypertriglyceridemic Pancreatitis.
- Published in:
- Application of Clinical Genetics, 2020, v. 13, p. 63, doi. 10.2147/TACG.S243148
- By:
- Publication type:
- Article
Reclassification of the HPGD p.Ala13Glu variant causing primary hypertrophic osteoarthropathy.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2023, v. 9, n. 4, p. 1, doi. 10.1101/mcs.a006291
- By:
- Publication type:
- Article
Clear cell renal carcinoma synchronous with dedifferentiated liposarcoma: a case report and review of the literature.
- Published in:
- 2020
- By:
- Publication type:
- journal article