P. Curfs

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.

B. Oostra, J. Fryns, C. D. de Die-Smulders, 1994, Human molecular genetics.

Dialogical Nursing Ethics: the Quality of Freedom Restrictions

G. Widdershoven, T. Abma, B. Frederiks, 2008, Nursing ethics.

Adaptive behavior in the fra(X) syndrome: a longitudinal study in eight patients.

J. Fryns, P. Curfs, G. Schreppers-Tijdink, 1989, American journal of medical genetics.

Establishing a difficult discrimination through time delay: Some critical dimensions of prompts

G. Lancioni, S. Striefel, P. Smeets, 1988 .