Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defects. Issue 1 (25th September 2018)

Record Type:: Journal Article
Title:: Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defects. Issue 1 (25th September 2018)
Main Title:: Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defects
Authors:: Bhatt, Nidhi
Loew, Jerome M.
Gallagher, Patrick
Mittal, Nupur
Abstract:
Is Part Of:: Pediatric blood & cancer. Volume 66:Issue 1(2019)
Journal:: Pediatric blood & cancer
Issue:: Volume 66:Issue 1(2019)
Issue Display:: Volume 66, Issue 1 (2019)
Year:: 2019
Volume:: 66
Issue:: 1
Issue Sort Value:: 2019-0066-0001-0000
Page Start:: n/a
Page End:: n/a
Publication Date:: 2018-09-25
Subjects:: alpha‐spectrin -- hereditary spherocytosis -- nondominant
Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/pbc.27480 ↗
Languages:: English
ISSNs:: 1545-5009
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 11312.xml