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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Springe zu: 2019 | 2018 | 2017
Anzahl der Publikationen: 5

2019

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Holth, Arild; Capella, Gabriel; Davidson, Ben; Evans, D. Gareth; Martins, Alexandra; Moller, Pal und Hovig, Eivind (2019): Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing. In: Scientific Reports, Bd. 9, 18555 [PDF, 1MB]

2018

Dominguez-Valentin, Mev; Evans, D. Gareth R.; Nakken, Sigve; Tubeuf, HLsne; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal und Hovig, Eivind (2018): Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds. In: Hereditary Cancer in Clinical Practice 16:4 [PDF, 1MB]

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal und Hovig, Eivind (2018): Identification of genetic variants for clinical management of familial colorectal tumors. In: BMC Medical Genetics 19:26 [PDF, 652kB]

Dominguez-Valentin, Mev; Nakken, Sigve; Tubeuf, Helene; Vodak, Daniel; Ekstrom, Per Olaf; Nissen, Anke M.; Morak, Monika; Holinski-Feder, Elke; Martins, Alexandra; Moller, Pal und Hovig, Eivind (2018): Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families. In: Familial Cancer, Bd. 17, Nr. 1: S. 141-153

2017

Morak, Monika; Käsbauer, Sarah; Kerscher, Martina; Massdorf, Trisari; Holinski-Feder, Elke; Laner, Andreas; Nissen, Anke M.; Benet-Pages, Anna; Schackert, Hans K. und Keller, Gisela (2017): Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6. In: Familial Cancer, Bd. 16, Nr. 4: S. 491-500

Diese Liste wurde am Sat Mar 23 22:37:06 2024 CET erstellt.