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American Journal of Medical Genetics|December 15, 1991
Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?A Spaepen, C Schrander-Stumpel, J P Fryns, et al.American Journal of Medical Genetics|April 20, 1999
Longitudinal changes in cognitive and adaptive behavior in fragile X females: a prospective multicenter analysisG S Fisch, N Carpenter, J J Holden, et al.Journal of Medical Genetics|January 15, 2003
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.American Journal of Medical Genetics|April 1, 1992
Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?G S Fisch, L R Shapiro, R Simensen, et al.American Journal of Medical Genetics|February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter studyG S Fisch, T Arinami, U Froster-Iskenius, et al.American Journal of Medical Genetics|May 1, 1994
Mosaic tetrasomy 8p in two patients: clinical data and review of the literatureC T Schrander-Stumpel, L C Govaerts, J J Engelen, et al.Pageof 4