reference/9875824

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9875824

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	685
issn	0007-1048 1365-2141
issueIdentifier	5
pageRange	682-685
publicationName	British Journal of Haematology
startingPage	682
bibliographicCitation	Dufour C, Capasso M, Svahn J, Marrone A, Haupt R, Bacigalupo A, Giordani L, Longoni D, Pillon M, Pistorio A, Di Michele P, Iori AP, Pongiglione C, Lanciotti M, Iolascon A; Associazione Italiana di Emato-Oncologia Pediatrica (AIEOP); Department of Hematology, Ospedale S. Martino, Genoa, Italy. Homozygosis for (12) CA repeats in the first intron of the human IFN-gamma gene is significantly associated with the risk of aplastic anaemia in Caucasian population. Br J Haematol. 2004 Sep;126(5):682–5. doi: 10.1111/j.1365-2141.2004.05102.x. PMID: 15327519.
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date	2004-08-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/j.1365-2141.2004.05102.x https://pubmed.ncbi.nlm.nih.gov/15327519
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Homozygosis for (12) CA repeats in the first intron of the human IFN‐γ gene is significantly associated with the risk of aplastic anaemia in Caucasian population
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Total number of triples: 60.