A. Wiegers

发表

A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experience.

J. Fryns, L. Curfs, A. Kleczkowska, 1988, Journal de genetique humaine.

A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.

B. Oostra, J. Fryns, L. Curfs, 1994, Genetic counseling.

Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys.

J. Fryns, L. Curfs, M. Borghgraef, 1989, Journal of medical genetics.

Strengths and weaknesses in the cognitive profile of youngsters with Prader‐Willi syndrome

J. Fryns, L. Curfs, M. Borghgraef, 1991, Clinical genetics.

Adaptive behavior in the fragile X syndrome: profile and development.

J. Fryns, L. Curfs, A. Wiegers, 1993, American journal of medical genetics.

Mental status of females with an FMR1 gene full mutation.

B. D. de Vries, A. V. D. van den Ouweland, B. Oostra, 1996, American journal of human genetics.

Mental Status and Fragile X Expression in Relation to FMR-1 Gene Mutation

B. Oostra, A. Verkerk, J. Fryns, 1993, European journal of human genetics : EJHG.

The 49,XXXXY syndrome: clinical and psychological findings in five patients.

J. Fryns, L. Curfs, M. Borghgraef, 2008, Journal of mental deficiency research.

Identical psychological profile and behaviour pattern in different types of mutation in the FMR‐1 region

J. Fryns, L. Curfs, A. Wiegers, 1993, Clinical genetics.

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.

A longitudinal study of intelligence in Dutch fragile X boys.

J. Fryns, L. Curfs, A. Wiegers, 1992, Birth defects original article series.