A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature. (2nd November 2017)

Record Type:: Journal Article
Title:: A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature. (2nd November 2017)
Main Title:: A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature
Authors:: Graziano, Claudio
Gusson, Elena
Severi, Giulia
Isidori, Federica
Wischmeijer, Anita
Brugnara, Milena
Seri, Marco
Rossi, Cesare
Abstract:
Is Part Of:: Ophthalmic genetics. Volume 38:Number 6(2017)
Journal:: Ophthalmic genetics
Issue:: Volume 38:Number 6(2017)
Issue Display:: Volume 38, Issue 6 (2017)
Year:: 2017
Volume:: 38
Issue:: 6
Issue Sort Value:: 2017-0038-0006-0000
Page Start:: 590
Page End:: 592
Publication Date:: 2017-11-02
Subjects:: Eye -- Diseases -- Genetic aspects -- Periodicals
Eye Diseases -- genetics -- Periodicals
Eye Diseases -- in infancy & childhood -- Periodicals
617.7
Journal URLs:: http://informahealthcare.com/loi/opg ↗
http://informahealthcare.com ↗
http://www.tandf.co.uk/journals/titles/13816810.asp ↗
DOI:: 10.1080/13816810.2017.1318927 ↗
Languages:: English
ISSNs:: 1381-6810
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6270.893000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 5389.xml