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M Shoukier, N Klein, B Auber, J Wickert, J Schröder, B Zoll, P Burfeind, I Bartels, EA Alsat, M Lingen, P Grzmil, S Schulze, J Keyser, D Weise, M Borchers, E Hobbiebrunken, M Röbl, J Gärtner, K Brockmann and B Zirn Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants? Clinical Genetics 83

Version of Record online: 21 FEB 2012 | DOI: 10.1111/j.1399-0004.2012.01850.x

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