Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood‐onset glaucoma. Issue 3 (28th September 2016)

Record Type:: Journal Article
Title:: Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood‐onset glaucoma. Issue 3 (28th September 2016)
Main Title:: Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood‐onset glaucoma
Authors:: Sergouniotis, Panagiotis I
Ellingford, Jamie M
O'Sullivan, James
Fenerty, Cecilia H
Black, Graeme C
Abstract:
Is Part Of:: Acta ophthalmologica. Volume 95:Issue 3(2017)
Journal:: Acta ophthalmologica
Issue:: Volume 95:Issue 3(2017)
Issue Display:: Volume 95, Issue 3 (2017)
Year:: 2017
Volume:: 95
Issue:: 3
Issue Sort Value:: 2017-0095-0003-0000
Page Start:: e249
Page End:: e250
Publication Date:: 2016-09-28
Subjects:: Ophthalmology -- Periodicals
617.7005
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1755-3768 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/aos.13246 ↗
Languages:: English
ISSNs:: 1755-375X
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0641.750500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 2499.xml