![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 4
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