Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). (19th April 2013)

Record Type:: Journal Article
Title:: Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). (19th April 2013)
Main Title:: Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome)
Authors:: Hoffer, JL
Fryssira, H
Konstantinidou, AE
Ropers, H−H
Tzschach, A
Abstract:
Is Part Of:: Clinical genetics. Volume 83:Number 1(2013:Jan.)
Journal:: Clinical genetics
Issue:: Volume 83:Number 1(2013:Jan.)
Issue Display:: Volume 83, Issue 1 (2013)
Year:: 2013
Volume:: 83
Issue:: 1
Issue Sort Value:: 2013-0083-0001-0000
Page Start:: 92
Page End:: 95
Publication Date:: 2013-04-19
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/j.1399-0004.2012.01880.x ↗
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:: 19314.xml