Novel de novo MYRF gene mutation: A possible cause for several clinically overlapping syndromes. (18th November 2020)

Record Type:: Journal Article
Title:: Novel de novo MYRF gene mutation: A possible cause for several clinically overlapping syndromes. (18th November 2020)
Main Title:: Novel de novo MYRF gene mutation: A possible cause for several clinically overlapping syndromes
Authors:: Tanaka, Hiroyuki
Isojima, Tsuyoshi
Kimura, Yuki
Inuzuka, Ryo
Kitanaka, Sachiko
Abstract:
Is Part Of:: Congenital anomalies. Volume 61:Number 2(2021)
Journal:: Congenital anomalies
Issue:: Volume 61:Number 2(2021)
Issue Display:: Volume 61, Issue 2 (2021)
Year:: 2021
Volume:: 61
Issue:: 2
Issue Sort Value:: 2021-0061-0002-0000
Page Start:: 68
Page End:: 69
Publication Date:: 2020-11-18
Subjects:: Abnormalities, Human -- Periodicals
616.043
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/cga ↗
DOI:: 10.1111/cga.12402 ↗
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:: 15867.xml