Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient. (28th September 2012)

Record Type:: Journal Article
Title:: Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient. (28th September 2012)
Main Title:: Identification of the CFTR p.Phe508Del founder mutation in the absence of a polythymidine 9T allele in a Hispanic patient
Authors:: Dharajiya, N
Chisholm, KM
Dietz, L
Sue Richards, C
Kharrazi, M
Schrijver, I
Abstract:
Is Part Of:: Clinical genetics. Volume 83:Number 6(2013:Jun.)
Journal:: Clinical genetics
Issue:: Volume 83:Number 6(2013:Jun.)
Issue Display:: Volume 83, Issue 6 (2013)
Year:: 2013
Volume:: 83
Issue:: 6
Issue Sort Value:: 2013-0083-0006-0000
Page Start:: 598
Page End:: 599
Publication Date:: 2012-09-28
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12012 ↗
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:: 4166.xml