Deletions of 9q21.3 including NTRK2 are associated with severe phenotype. (27th October 2014)

Record Type:: Journal Article
Title:: Deletions of 9q21.3 including NTRK2 are associated with severe phenotype. (27th October 2014)
Main Title:: Deletions of 9q21.3 including NTRK2 are associated with severe phenotype
Authors:: Hancarova, Miroslava
Puchmajerova, Alena
Drabova, Jana
Karaskova, Eliska
Vlckova, Marketa
Sedlacek, Zdenek
Abstract:
Is Part Of:: American journal of medical genetics. Volume 167:Number 1(2015:Jan.)
Journal:: American journal of medical genetics
Issue:: Volume 167:Number 1(2015:Jan.)
Issue Display:: Volume 167, Issue 1 (2015)
Year:: 2015
Volume:: 167
Issue:: 1
Issue Sort Value:: 2015-0167-0001-0000
Page Start:: 264
Page End:: 267
Publication Date:: 2014-10-27
Subjects:: Medical genetics -- Periodicals
616.14205
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/ajmg.a.36797 ↗
Languages:: English
ISSNs:: 1552-4825
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 3289.xml