Jean Steyaert

Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency

J. Steyaert, G. Matthijs, R. Wevers, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

DISC1 duplication in two brothers with autism and mild mental retardation

H. Peeters, J. Breckpot, A. Crepel, 2010, Clinical genetics.

Molecular-intelligence correlations in young fragile X males with a mild CGG repeat expansion in the FMR1 gene.

J. Steyaert, J. Fryns, E. Legius, 1996, American journal of medical genetics.

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion

B. Franke, H. Smeets, J. Steyaert, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism

K. Devriendt, J. Steyaert, W. V. D. Van de Ven, 2003, Journal of medical genetics.

The XYY syndrome: a follow-up study on 38 boys.

J. Steyaert, J. Fryns, M. Geerts, 2003, Genetic counseling.

Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence.

J. Steyaert, J. Fryns, E. Legius, 1995, Journal of neurology, neurosurgery, and psychiatry.