reference/3791179

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3791179

Outgoing Links

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endingPage	1099
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publicationName	European journal of human genetics : EJHG
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bibliographicCitation	Whibley A, Urquhart J, Dore J, Willatt L, Parkin G, Gaunt L, Black G, Donnai D, Raymond FL. Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements. European Journal of Human Genetics. 2010 May 19;18(10):1095–9. doi: 10.1038/ejhg.2010.41.
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date	2010-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC2987451 https://pubmed.ncbi.nlm.nih.gov/20485326 https://doi.org/10.1038/ejhg.2010.41
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements
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Total number of triples: 51.