reference/18584288

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publicationName	Human Molecular Genetics
startingPage	2837
bibliographicCitation	Siitonen HA, Kopra O, Kääriäinen H, Haravuori H, Winter RM, Säämänen AM, Peltonen L, Kestilä M. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. Hum Mol Genet. 2003 Nov 01;12(21):2837–44. doi: 10.1093/hmg/ddg306. PMID: 12952869.
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date	2003-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
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title	Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases
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