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publicationName Nature Genetics
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bibliographicCitation Koolen DA, Kramer JM, Neveling K, Nillesen WM, Moore-Barton HL, Elmslie FV, Toutain A, Amiel J, Malan V, Tsai AC, Cheung SW, Gilissen C, Verwiel ET, Martens S, Feuth T, Bongers EM, de Vries P, Scheffer H, Vissers LE, de Brouwer AP, Brunner HG, Veltman JA, Schenck A, Yntema HG, de Vries BB. Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. Nat Genet. 2012 Apr 29;44(6):639–41. doi: 10.1038/ng.2262. PMID: 22544363.
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date 2012-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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title Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome
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