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

Renée Zwanenburg (Contributor)
Selma A.J. Ruiter (Creator)
Edwin R Van den Heuvel (Contributor)
Boudien C.T. 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)

Datum van beschikbaarheid	26-apr-2016
Uitgever	figshare

Contact

[email protected]

DOI
10.6084/m9.figshare.c.3631301_d1

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 blz., 16.
Onderzoeksoutput: Article › Academic › peer review

Open Access
Bestand
63 Citaten (Scopus)

376 Downloads (Pure)

Citeer dit

DataSetCite

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

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

Description

Contact

DOI

Onderzoekersoutput

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

Citeer dit