Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: A systematic and prospective study in 34 children

Renée J Zwanenburg, Selma A J Ruiter, Edwin R van den Heuvel, Boudien C T Flapper, Conny M A Van Ravenswaaij-Arts

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Additional file 2: Table S1. of Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children
Zwanenburg, R. J. (Contributor), Ruiter, S. A. J. (Contributor), Van Den Heuvel, E. R. (Contributor), Flapper, B. C. T. (Contributor) & Van Ravenswaaij-Arts, C. M. A. (Contributor), University of Groningen, 15-Dec-2016
DOI: 10.6084/m9.figshare.c.3631301_d1.v1, https://doi.org/10.6084%2Fm9.figshare.c.3631301_d1.v1
Dataset
Additional file 2: Table S1. of Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children
Zwanenburg, R. (Contributor), Ruiter, S. A. J. (Creator), Van Den Heuvel, E. R. (Contributor), Flapper, B. C. T. (Contributor) & Van Ravenswaaij-Arts, C. M. A. (Contributor), figshare, 26-Apr-2016
DOI: 10.6084/m9.figshare.c.3631301_d1
Dataset