A novel stop codon variant affecting ΔNp63 isoforms associated with non‐syndromic limb‐mammary phenotype and uterine cervix dysplasia. Issue 3 (1st December 2020)

Record Type:: Journal Article
Title:: A novel stop codon variant affecting ΔNp63 isoforms associated with non‐syndromic limb‐mammary phenotype and uterine cervix dysplasia. Issue 3 (1st December 2020)
Main Title:: A novel stop codon variant affecting ΔNp63 isoforms associated with non‐syndromic limb‐mammary phenotype and uterine cervix dysplasia
Authors:: Guazzarotti, Laura
Sani, Ilaria
Giglio, Sabrina
Brunello, Francesco
Perilongo, Giorgio
Bocciardi, Renata
Abstract:
Is Part Of:: Clinical genetics. Volume 99:Issue 3(2021)
Journal:: Clinical genetics
Issue:: Volume 99:Issue 3(2021)
Issue Display:: Volume 99, Issue 3 (2021)
Year:: 2021
Volume:: 99
Issue:: 3
Issue Sort Value:: 2021-0099-0003-0000
Page Start:: 486
Page End:: 487
Publication Date:: 2020-12-01
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13889 ↗
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:: 22198.xml