- Brooke-Spiegler syndrome: report of 10 patients from 8 families with novel germline mutations2010 | Ústřední knihovna
- Brooke-Spiegler syndrome: report of 10 patients from 8 families with novel germline mutations2010 | Lékařská fakulta v Plzni
- Mendelian nightmares: The germline-restricted chromosome of songbirds2022 | Přírodovědecká fakulta
- Rare deleterious germline variants and risk of lung cancer2021 | 2. lékařská fakulta
- Overview on population screening for carriers with germline BRCA mutation in China2022 | Lékařská fakulta v Plzni
- Germline multigene panel testing of patients with endometrial cancer2023 | Lékařská fakulta v Plzni, 1. lékařská fakulta, Přírodovědecká fakulta
- Double germline mutations in the RET proto-oncogene in MEN 2A and MEN 2B kindreds2006 | 2. lékařská fakulta
- CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate2020 | 1. lékařská fakulta
- Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds2006 | Ústřední knihovna, Lékařská fakulta v Hradci Králové
- Double Germline Mutations in the RET Proto-oncogene in MEN 2A and MEN 2B Kindreds2006 | Ústřední knihovna, Lékařská fakulta v Hradci Králové, 2. lékařská fakulta, 1. lékařská fakulta
- A novel c. 204 Ile68Met germline variant in exon 2 of the mutL homolog 1 gene in a colorectal cancer patient2015 | 1. lékařská fakulta
- Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer2009 | 2. lékařská fakulta
- Micro Germline-Restricted Chromosome in Blue Tits: Evidence for Meiotic Functions2023 | Přírodovědecká fakulta
- Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer2019 | 1. lékařská fakulta
- Germline-restricted chromosome shows remarkable variation in size among closely related passerine species2022 | Přírodovědecká fakulta
- A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer2020 | Lékařská fakulta v Plzni
- A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer2021 | Lékařská fakulta v Plzni
- Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations2005 | 2. lékařská fakulta, 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer2022 | Lékařská fakulta v Plzni
- Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer2022 | Lékařská fakulta v Plzni
- Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants2023 | 1. lékařská fakulta
- Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency2022 | 2. lékařská fakulta
- Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement2023 | 1. lékařská fakulta
- Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age2007 | 2. lékařská fakulta, 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Germline mutation in the TP53 gene in uveal melanoma2018 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours1998 | 2. lékařská fakulta
- ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk2023 | Ústřední knihovna, 1. lékařská fakulta
- Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients2021 | 1. lékařská fakulta
- A case of Brooke-Spiegler syndrome with a novel germline deep intronic mutation in the CYLD gene leading to intronic exonization, diverse somatic mutations, and unusual histology2009 | Lékařská fakulta v Plzni, 1. lékařská fakulta
- Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes2020 | Ústřední knihovna, 1. lékařská fakulta