Additional file 2: Table S1. of Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children

Renée J. Zwanenburg (Contributor)
Selma A.J. Ruiter (Contributor)
Edwin R van den Heuvel (Contributor)
Boudien Flapper (Contributor)
Conny van Ravenswaaij-Arts (Contributor)

Clinical Cognitive Neuropsychiatry Research Program (CCNP)

Dataset

Description

Bayley-III-NL developmental age-equivalents (DAEs) and developmental quotients (DQs) for cognition separated by gender. (XLS 18.0 kb)

Date made available	15-Dec-2016
Publisher	University of Groningen

Keywords on Datasets

phelan-McDermid Syndrome
22q13 deletion syndrome
SHANK3
Intellectual disability
Autism
Neurodevelopmental disorders
Developmental phenotype

Contact

researchdata@rug.nl

DOI
10.6084/m9.figshare.c.3631301_d1.v1

Access Dataset

https://doi.org/10.6084%2Fm9.figshare.c.3631301_d1.v1

1 Article

Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: A systematic and prospective study in 34 children
Zwanenburg, R. J., Ruiter, S. A. J., van den Heuvel, E. R., Flapper, B. C. T. & Van Ravenswaaij-Arts, C. M. A., 26-Apr-2016, In: Journal of neurodevelopmental disorders. 8, 12 p., 16.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
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268 Downloads (Pure)

Cite this

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) (15-Dec-2016). Additional file 2: Table S1. of Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children. University of Groningen. 10.6084/m9.figshare.c.3631301_d1.v1