reference/30380711

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30380711

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publicationName	Journal of thrombosis and haemostasis : JTH
startingPage	1988
bibliographicCitation	Jourdy Y, Chatron N, Carage M‐, Fretigny M, Meunier S, Zawadzki C, Gay V, Negrier C, Sanlaville D, Vinciguerra C. Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability. Journal of Thrombosis and Haemostasis. 2016 Oct;14(10):1988–93. doi: 10.1111/jth.13430.
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date	201610
identifier	https://doi.org/10.1111/jth.13430 https://pubmed.ncbi.nlm.nih.gov/27477789
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
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