reference/19282604

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19282604

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, U.S. Gov't, P.H.S.
endingPage	700
issn	0022-3476
issueIdentifier	5
pageRange	695-700
publicationName	The Journal of Pediatrics
startingPage	695
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bibliographicCitation	Enns GM, Steiner RD, Buist N, Cowan C, Leppig KA, McCracken MF, Westphal V, Freeze HH, O'Brien JF, Jaeken J, Matthijs G, Behera S, Hudgins L. Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins. The Journal of Pediatrics. 2002 Nov;141(5):695–700. doi: 10.1067/mpd.2002.128658.
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date	200211
identifier	https://doi.org/10.1067/mpd.2002.128658 https://pubmed.ncbi.nlm.nih.gov/12410200
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins
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Total number of triples: 51.