XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans. Issue 3 (29th November 2018)

Record Type:: Journal Article
Title:: XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans. Issue 3 (29th November 2018)
Main Title:: XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans
Authors:: Zhang, Ya‐Xin
Li, Hai‐Yu
He, Wen‐Bin
Tu, Chaofeng
Du, Juan
Li, Wen
Lu, Guang‐Xiu
Lin, Ge
Yang, Yongjia
Tan, Yue‐Qiu
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 95:Issue 3(2019)
Journal:: Clinical genetics
Issue:: Volume 95:Issue 3(2019)
Issue Display:: Volume 95, Issue 3 (2019)
Year:: 2019
Volume:: 95
Issue:: 3
Issue Sort Value:: 2019-0095-0003-0000
Page Start:: 442
Page End:: 443
Publication Date:: 2018-11-29
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13475 ↗
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:: 11709.xml