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

Crossref DOI link: https://doi.org/10.1186/s11689-016-9150-0

Published Online: 2016-04-26

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Zwanenburg, Renée J.

Ruiter, Selma A.J.

van den Heuvel, Edwin R.

Flapper, Boudien C.T.

Van Ravenswaaij-Arts, Conny M.A.
Funding

Funding for this research was provided by:

Netherlands Organisation for Health Research and Development (NL) (113-20-2009)

Netherlands Organisation for Health Research and Development (NL) (15701.3002)