20102017

Research output per year

If you made any changes in Pure these will be visible here soon.

Research Output

A novel mutation in L1CAM causes a mild form of L1 syndrome: a case report

Otter, M., Wevers, M., Pisters, M., Pfundt, R., Vos, Y., Nievelstein, R. J. & Stumpel, C., Aug 2017, In : Clinical Case Reports. 5, 8, p. 1213-1217 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

The psychiatric phenotype in triple X syndrome: New hypotheses illustrated in two cases

Otter, M., Schrander-Stumpel, C. T. R. M., Didden, R. & Curfs, L. M. G., 2012, In : Developmental Neurorehabilitation. 15, 3, p. 233-238

Research output: Contribution to journalArticleAcademicpeer-review

Triple X syndrome: a review of the literature

Otter, M., Schrander-Stumpel, C. T. R. M. & Curfs, L. M. G., Mar 2010, In : European Journal of Human Genetics. 18, 3, p. 265-271

Research output: Contribution to journalArticleAcademicpeer-review