Novel sequence variants in the MKKS gene cause Bardet‐Biedl syndrome with intra‐ and inter‐familial variable phenotypes. (22nd December 2017)

Record Type:: Journal Article
Title:: Novel sequence variants in the MKKS gene cause Bardet‐Biedl syndrome with intra‐ and inter‐familial variable phenotypes. (22nd December 2017)
Main Title:: Novel sequence variants in the MKKS gene cause Bardet‐Biedl syndrome with intra‐ and inter‐familial variable phenotypes
Authors:: Ullah, Asmat
Khalid, Maryam
Umair, Muhammad
Khan, Sher Alam
Bilal, Muhammad
Khan, Saadullah
Ahmad, Wasim
Abstract:
Is Part Of:: Congenital anomalies. Volume 58:Number 5(2018)
Journal:: Congenital anomalies
Issue:: Volume 58:Number 5(2018)
Issue Display:: Volume 58, Issue 5 (2018)
Year:: 2018
Volume:: 58
Issue:: 5
Issue Sort Value:: 2018-0058-0005-0000
Page Start:: 173
Page End:: 175
Publication Date:: 2017-12-22
Subjects:: Abnormalities, Human -- Periodicals
616.043
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗
DOI:: 10.1111/cga.12264 ↗
Languages:: English
ISSNs:: 0914-3505
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3410.683000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 7181.xml