NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome. Issue 1 (29th March 2021)

Record Type:: Journal Article
Title:: NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome. Issue 1 (29th March 2021)
Main Title:: NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
Authors:: Cavaliere, Elena
Gortan, Anna Jolanda
Passon, Nadia
Fabbro, Dora
Marin, Dario
Carecchio, Miryam
Baldan, Federica
Credendino, Sara Carmela
Gallo, Rosa
Cogo, Paola
Damante, Giuseppe
De Vita, Gabriella
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 100:Issue 1(2021)
Journal:: Clinical genetics
Issue:: Volume 100:Issue 1(2021)
Issue Display:: Volume 100, Issue 1 (2021)
Year:: 2021
Volume:: 100
Issue:: 1
Issue Sort Value:: 2021-0100-0001-0000
Page Start:: 114
Page End:: 116
Publication Date:: 2021-03-29
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13961 ↗
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:: 17525.xml