Clinical insights and molecular study of three foetuses with DYNC2H1 gene mutation causing short rib thoracic dystrophy. Issue 6 (11th March 2021)

Record Type:: Journal Article
Title:: Clinical insights and molecular study of three foetuses with DYNC2H1 gene mutation causing short rib thoracic dystrophy. Issue 6 (11th March 2021)
Main Title:: Clinical insights and molecular study of three foetuses with DYNC2H1 gene mutation causing short rib thoracic dystrophy
Authors:: Thakur, Seema
Gupta, Rachna
Bansal, Deepak
Singh, Chanchal
Agarwal, Divya
Saxena, Kamal Kant
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 99:Issue 6(2021)
Journal:: Clinical genetics
Issue:: Volume 99:Issue 6(2021)
Issue Display:: Volume 99, Issue 6 (2021)
Year:: 2021
Volume:: 99
Issue:: 6
Issue Sort Value:: 2021-0099-0006-0000
Page Start:: 853
Page End:: 854
Publication Date:: 2021-03-11
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13953 ↗
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:: 16739.xml