Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features. (April 2014)

Record Type:: Journal Article
Title:: Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features. (April 2014)
Main Title:: Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features
Authors:: Valdivielso‐Ramos, M.
Solera, J.
Mauleon, C.
Hernanz, J. M.
Amiñoso, C.
Galiano, S.
De, P.
Abstract:
Is Part Of:: Clinical and experimental dermatology. Volume 39:Number 3(2014)
Journal:: Clinical and experimental dermatology
Issue:: Volume 39:Number 3(2014)
Issue Display:: Volume 39, Issue 3 (2014)
Year:: 2014
Volume:: 39
Issue:: 3
Issue Sort Value:: 2014-0039-0003-0000
Page Start:: 406
Page End:: 407
Publication Date:: 2014-04
Subjects:: Skin -- Diseases -- Periodicals
616.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2230 ↗
https://academic.oup.com/ced/issue ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ced.12291 ↗
Languages:: English
ISSNs:: 0307-6938
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.250000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 4303.xml