Anzahl der Publikationen: 4
Zeitschriftenartikel
Morak, Monika; Steinke-Lange, Verena; Massdorf, Trisari; Benet-Pages, Anna; Locher, Melanie; Laner, Andreas; Kayser, Katrin; Aretz, Stefan und Holinski-Feder, Elke
(2020):
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics.
In: Familial Cancer, Bd. 19, Nr. 2: S. 161-167
Morak, Monika; Schäfer, Kerstin; Steinke-Lange, Verena; Köhler, Udo; Keinath, Susanne; Massdorf, Trisari; Mauracher, Brigitte; Rahner, Nils; Bailey, Jessica; Kling, Christiane; Haeusser, Tanja; Laner, Andreas und Holinski-Feder, Elke
(2019):
Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genes.
In: European Journal of Human Genetics, Bd. 27, Nr. 12: S. 1808-1820
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
Morak, Monika; Koehler, Udo; Schackert, Hans Konrad; Steinke, Verena; Royer-Pokora, Brigitte; Schulmann, Karsten; Kloor, Matthias; Höchter, Wilhelm; Weingart, Josef; Keiling, Cortina; Massdorf, Trisari und Holinski-Feder, Elke
(August 2011):
Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome.
In: Journal of medical genetics, Bd. 48, Nr. 8: S. 513-519
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