A. Spaepen

Are patients with Down syndrome vulnerable to life-threatening COVID-19?

H. D. De Cauwer, A. Spaepen, 2020, Acta Neurologica Belgica.

A severe case of mandibuloacral dysplasia in a girl.

J. Fryns, C. Schrander-Stumpel, J. Dumon, 1992, American journal of medical genetics.

The variable clinical spectrum and mental prognosis of the acrocallosal syndrome.

J. Fryns, H. van den Berghe, P. Casaer, 1991, Journal of medical genetics.

Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?

J. Fryns, C. D. de Die-Smulders, H. van den Berghe, 1991, American journal of medical genetics.

X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.

J. Fryns, J. Cassiman, H. van den Berghe, 1991, Journal of medical genetics.

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

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

MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

J. Fryns, E. Legius, J. Cassiman, 1992, Journal of medical genetics.

Neurofibromatosis type 1 in childhood: a study of the neuropsychological profile in 45 children.

J. Fryns, E. Legius, P. Casaer, 1994, Genetic counseling.