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Anzahl der Publikationen: 5
Zeitschriftenartikel
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]
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
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