Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. (27th December 2013)

Record Type:: Journal Article
Title:: Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. (27th December 2013)
Main Title:: Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction
Authors:: Foster, J.
Kapoor, S.
Diaz‐Horta, O.
Singh, A.
Abad, C.
Rastogi, A.
Moharana, R.
Tekeli, O.
Walz, K.
Tekin, M.
Abstract:
Is Part Of:: Clinical genetics. Volume 86:Number 6(2014:Dec.)
Journal:: Clinical genetics
Issue:: Volume 86:Number 6(2014:Dec.)
Issue Display:: Volume 86, Issue 6 (2014)
Year:: 2014
Volume:: 86
Issue:: 6
Issue Sort Value:: 2014-0086-0006-0000
Page Start:: 589
Page End:: 591
Publication Date:: 2013-12-27
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12321 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 3207.xml