reference/6812036

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6812036

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bibliographicCitation	Giangiobbe S, Caraffi SG, Ivanovski I, Maini I, Pollazzon M, Rosato S, Trimarchi G, Lauriello A, Marinelli M, Nicoli D, Baldo C, Laurie S, Flores‐Daboub J, Provenzano A, Andreucci E, Peluso F, Rizzo R, Stewart H, Lachlan K, Bayat A, Napoli M, Carboni G, Baker J, Mendel A, Piatelli G, Pantaleoni C, Mattina T, Prontera P, Mendelsohn NJ, Giglio S, Zuffardi O, Garavelli L. Expanding the phenotype of Wiedemann‐Steiner syndrome: Craniovertebral junction anomalies. American J of Med Genetics Pt A. 2020 Oct 11;182(12):2877–86. doi: 10.1002/ajmg.a.61859.
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date	2020-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ajmg.a.61859 https://pubmed.ncbi.nlm.nih.gov/33043602
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Expanding the phenotype of Wiedemann‐Steiner syndrome: Craniovertebral junction anomalies
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