1. Comprehensive Evaluation of Commercial Bisulfite-Based DNA Methylation Kits and Development of an Alternative Protocol With Improved Conversion Performance. (22nd March 2018) Authors: Tierling, Sascha; Schmitt, Beate; Walter, Jörn Journal: Genetics & epigenetics Issue: Volume 10(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Patient with Marfan Syndrome and a Novel Variant in FBN1 Presenting with Bilateral Popliteal Artery Aneurysm. (29th March 2018) Authors: Mohammad, Ahmed; Helmi, Haytham; Atwal, Paldeep S. Other Names: Cotter Philip D. Academic Editor. Journal: Case reports in genetics Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. How Mongolia's milk-based empire got its start. (15th November 2018) Journal: Nature Issue: Volume 563:Number 7731(2018) Page Start: 296 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. China's crackdown on genetics breaches could deter data sharing. (15th November 2018) Authors: Cyranoski, David Journal: Nature Issue: Volume 563:Number 7731(2018) Page Start: 301 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. China's crackdown on genetics breaches could deter data sharing. (15th November 2018) Authors: Cyranoski, David Journal: Nature Issue: Volume 563:Number 7731(2018) Page Start: 301 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. How Mongolia's milk-based empire got its start. (15th November 2018) Journal: Nature Issue: Volume 563:Number 7731(2018) Page Start: 296 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identifying a Novel DPYD Polymorphism Associated with Severe Toxicity to 5-FU Chemotherapy in a Saudi Patient. (21st August 2019) Authors: Bukhari, Nedal; Azam, Faisal; Alfawaz, Mohammed; Zahrani, Mohammed Other Names: Yapijakis Christos Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Increasing Evidence for the Association of Breast Implant-Associated Anaplastic Large Cell Lymphoma and Li Fraumeni Syndrome. (16th July 2019) Authors: Adlard, Julian; Burton, Cathy; Turton, Philip Other Names: Yapijakis Christos Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Resolving a Multi-Generational Neuromuscular Mystery in a Family Presenting with a Variable Scapuloperoneal Syndrome in a c.464G>A, p.Arg155His VCP Mutation. (9th October 2019) Authors: Jerath, Nivedita U. Other Names: Cotter Philip D. Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome. (28th July 2019) Authors: Askaner, Gustav; Lei, Ulrikke; Bertelsen, Birgitte; Venzo, Alessandro; Wadt, Karin Other Names: Yapijakis Christos Academic Editor. Journal: Case reports in genetics Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗