Predicate |
Object |
contentType |
Case Reports|Journal Article|Research Support, U.S. Gov't, P.H.S. |
endingPage |
37 |
issn |
0022-3476 |
issueIdentifier |
1 |
pageRange |
33-37 |
publicationName |
The Journal of Pediatrics |
startingPage |
33 |
bibliographicCitation |
Witemeyer S, Van Epps DE. A familial defect in cellular chemotaxis associated with redheadedness and recurrent infection. The Journal of Pediatrics. 1976 Jul;89(1):33–7. doi: 10.1016/s0022-3476(76)80922-5. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_61fcfe1e05cac2bc748befa02859507c http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f4a405a6613326666dbcddf78f1308ed |
date |
197607 |
identifier |
https://pubmed.ncbi.nlm.nih.gov/932900 https://doi.org/10.1016/s0022-3476%2876%2980922-5 |
isPartOf |
https://portal.issn.org/resource/ISSN/0022-3476 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5127 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
A familial defect in cellular chemotaxis associated with redheadedness and recurrent infection |
discusses |
http://id.nlm.nih.gov/mesh/M0004928 |
hasPrimarySubjectTerm |
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hasSubjectTerm |
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discussesAsDerivedByTextMining |
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