A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly. Issue 4 (8th January 2019)

Record Type:: Journal Article
Title:: A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly. Issue 4 (8th January 2019)
Main Title:: A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly
Authors:: Ullah, Asmat
Umair, Muhammad
Majeed, Ayesha I.
Abdullah,
Jan, Abid
Ahmad, Wasim
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 95:Issue 4(2019)
Journal:: Clinical genetics
Issue:: Volume 95:Issue 4(2019)
Issue Display:: Volume 95, Issue 4 (2019)
Year:: 2019
Volume:: 95
Issue:: 4
Issue Sort Value:: 2019-0095-0004-0000
Page Start:: 540
Page End:: 541
Publication Date:: 2019-01-08
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13495 ↗
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:: 10443.xml