Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. Issue 8 (12th May 2016)

Record Type:: Journal Article
Title:: Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. Issue 8 (12th May 2016)
Main Title:: Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis
Authors:: Prasad, Rathi
Brewer, Carole
Burren, Christine P.
Abstract:
Is Part Of:: American journal of medical genetics. Volume 170:Issue 8(2016)
Journal:: American journal of medical genetics
Issue:: Volume 170:Issue 8(2016)
Issue Display:: Volume 170, Issue 8 (2016)
Year:: 2016
Volume:: 170
Issue:: 8
Issue Sort Value:: 2016-0170-0008-0000
Page Start:: 2222
Page End:: 2225
Publication Date:: 2016-05-12
Subjects:: Medical genetics -- Periodicals
616.14205
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/ajmg.a.37731 ↗
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:: 1623.xml