reference/31146234

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31146234

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publicationName	European journal of human genetics : EJHG
startingPage	88
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bibliographicCitation	Di Fede E, Massa V, Augello B, Squeo G, Scarano E, Perri AM, Fischetto R, Causio FA, Zampino G, Piccione M, Curridori E, Mazza T, Castellana S, Larizza L, Ghelma F, Colombo EA, Gandini MC, Castori M, Merla G, Milani D, Gervasini C. Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes. European Journal of Human Genetics. 2020 Jul 08;29(1):88–98. doi: 10.1038/s41431-020-0679-8.
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date	2020-07-08^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
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