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Clinical Genetics|October 1, 1989
Spondylocostal dysostosis: an example of autosomal dominant transmission in a large familyE Floor, R O De Jong, J P Fryns, et al.Journal De Genetique Humaine|December 1, 1983
Ring chromosome 14. A distinct clinical entityJ P Fryns, E Kubien, A Kleczkowska, et al.Journal De Genetique Humaine|March 1, 1980
Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boyJ P Fryns, L Emmery, J Timmermans, et al.Annales De Genetique|January 1, 1982
8p trisomy in a malformed foetusJ P Fryns, P Petit, F Moerman, et al.Annales De Genetique|January 1, 1980
Carpal and tarsal osteolysisJ P Fryns, J C Pedersen, D Hauglustaine, et al.Clinical Genetics|December 1, 1987
A peculiar subphenotype in the fra(X) syndrome: extreme obesity-short stature-stubby hands and feet-diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome?J P Fryns, M Haspeslagh, A M Dereymaeker, et al.Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestationsG Vantrappen, N Rommel, A Swillen, et al.Acta Oto-Rhino-Laryngologica Belgica|January 1, 1991
On the etiology of hearing loss in a population of 155 institutionalized childrenA M Dereymaeker, J P Fryns, B Ars, et al.Neuropsychologia|October 20, 2006
Mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.Cancer Genetics and Cytogenetics|October 1, 1990
No significant increase in spontaneous and ethyl methane sulfonate-induced sister chromatid exchanges at the Xq27.3 fragile siteT Lukusa, E Meulepas, J P Fryns, et al.Pageof 89