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Author/Creator Vaeth, Signe

1. Rothmund–Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene. Issue 3 (24th February 2016)

Authors:
Suter, Aude‐Annick; Itin, Peter; Heinimann, Karl; Ahmed, Munaza; Ashraf, Tazeen; Fryssira, Helen; Kini, Usha; Lapunzina, Pablo; Miny, Peter; Sommerlund, Mette; Suri, Mohnish; Vaeth, Signe; Vasudevan, Pradeep; Gallati, Sabina
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 4:Issue 3(2016)
Page Start:
359
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Magnetic resonance neurography and diffusion tensor imaging of the peripheral nerves in patients with Charcot‐Marie‐Tooth Type 1A. Issue 6 (29th May 2017)

Authors:
Vaeggemose, Michael; Vaeth, Signe; Pham, Mirko; Ringgaard, Steffen; Jensen, Uffe B.; Tankisi, Hatice; Ejskjaer, Niels; Heiland, Sabine; Andersen, Henning
Journal:
Muscle & nerve
Issue:
Volume 56:Issue 6(2017)
Page Start:
E78
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗