Related Articles
Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype
Importance of multigene panel test in patients with consanguineous marriage and family history of breast cancer
Next‑generation sequencing of BRCA1 and BRCA2 in breast cancer patients and control subjects
Secondary leiomyosarcoma of the nasal cavity in a treated patient with possible hereditary retinoblastoma with germline reciprocal translocation of RB1 and DMXL1 and somatic TP53 mutation: A case report
Germline and somatic c-met mutations in multifocal/bilateral and sporadic papillary renal carcinomas of selected patients