FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review. (July 2016)

Record Type:: Journal Article
Title:: FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review. (July 2016)
Main Title:: FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review
Authors:: Goel, Dimple
Oei, Ju Lee
Shand, Antonia W
Mowat, David
Loo, Christine
Abstract:
Is Part Of:: Journal of paediatrics and child health. Volume 52:Number 7(2016:Jul.)
Journal:: Journal of paediatrics and child health
Issue:: Volume 52:Number 7(2016:Jul.)
Issue Display:: Volume 52, Issue 7 (2016)
Year:: 2016
Volume:: 52
Issue:: 7
Issue Sort Value:: 2016-0052-0007-0000
Page Start:: 787
Page End:: 788
Publication Date:: 2016-07
Subjects:: Children -- Health and hygiene -- Periodicals
Pediatrics -- Periodicals
618.92
Journal URLs:: http://www.blackwellpublishing.com/aims.asp?ref=1034-4810&site=1 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/jpc.13191 ↗
Languages:: English
ISSNs:: 1034-4810
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 5027.778000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 2858.xml