Author/Creator: Mulley, John C - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Mulley, John C

1. De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. Issue 2 (8th July 2009)

Authors:: Heron, Sarah E; Scheffer, Ingrid E; Iona, Xenia; Zuberi, Sameer M; Birch, Rachael; McMahon, Jacinta M; Bruce, Carla M; Berkovic, Samuel F; Mulley, John C
Journal:: Journal of medical genetics
Issue:: Volume 47:Issue 2(2010)
Page Start:: 137
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients. Issue 1 (23rd October 2010)

Authors:: Conlin, Laura K; Kramer, Whitney; Hutchinson, Anne L; Li, Xia; Riethman, Harold; Hakonarson, Hakon; Mulley, John C; Scheffer, Ingrid E; Berkovic, Samuel F; Hosain, Syed A; Spinner, Nancy B
Journal:: Journal of medical genetics
Issue:: Volume 48:Issue 1(2011)
Page Start:: 1
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗