No major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders. Issue 1 (8th October 2015)

Record Type:: Journal Article
Title:: No major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders. Issue 1 (8th October 2015)
Main Title:: No major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders
Authors:: Müller, Anne
Soellner, Lukas
Binder, Gerhard
Begemann, Matthias
Eggermann, Thomas
Abstract:
Is Part Of:: American journal of medical genetics. Volume 170:Issue 1(2016)
Journal:: American journal of medical genetics
Issue:: Volume 170:Issue 1(2016)
Issue Display:: Volume 170, Issue 1 (2016)
Year:: 2016
Volume:: 170
Issue:: 1
Issue Sort Value:: 2016-0170-0001-0000
Page Start:: 283
Page End:: 284
Publication Date:: 2015-10-08
Subjects:: Silver–Russell syndrome -- Beckwith–Wiedemann syndrome -- IGF2 mutations
Medical genetics -- Periodicals
616.14205
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/ajmg.a.37416 ↗
Languages:: English
ISSNs:: 1552-4825
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 1438.xml