Author/Creator: Begemann, M. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Begemann, M.

1. Isolated hypermethylation of GRB10 (7p12.2) in a Silver–Russell syndrome patient carrying a 20p13 microdeletion. (10th June 2013)

Authors:: Eggermann, T.; Schneider‐Rätzke, B.; Begemann, M.; Spengler, S.
Journal:: Clinical genetics
Issue:: Volume 85:Number 4(2014:Apr.)
Page Start:: 399
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself. Issue 1 (8th March 2017)

Authors:: Scheuvens, R.; Begemann, M.; Soellner, L.; Meschede, D.; Raabe‐Meyer, G.; Elbracht, M.; Schubert, R.; Eggermann, T.
Journal:: Clinical genetics
Issue:: Volume 92:Issue 1(2017)
Page Start:: 45
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Recent Advances in Imprinting Disorders. Issue 1 (4th August 2016)

Authors:: Soellner, L.; Begemann, M.; Mackay, D.J.G.; Grønskov, K.; Tümer, Z.; Maher, E.R.; Temple, I.K.; Monk, D.; Riccio, A.; Linglart, A.; Netchine, I.; Eggermann, T.
Journal:: Clinical genetics
Issue:: Volume 91:Issue 1(2017)
Page Start:: 3
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing. Issue 5 (October 2015)

Authors:: Knopp, C.; Rudnik-Schöneborn, S.; Eggermann, T.; Bergmann, C.; Begemann, M.; Schoner, K.; Zerres, K.; Ortiz Brüchle, N.
Journal:: Molecular and cellular probes
Issue:: Volume 29:Issue 5(2015)
Page Start:: 299
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗