Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A.

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Published in Mol Syndromol on September 14, 2010

Authors

R Oegema1, A de Klein, A J Verkerk, R Schot, B Dumee, H Douben, B Eussen, L Dubbel, P J Poddighe, I van der Laar, W B Dobyns, P J van der Spek, M H Lequin, I F M de Coo, M-C Y de Wit, M W Wessels, G M S Mancini

Author Affiliations

1: Department of Clinical Genetics, Rotterdam, The Netherlands.

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