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American Journal of Medical Genetics. Part A|December 4, 2004
Rett syndrome in females with CTS hot spot deletions: a disorder profileE Smeets, P Terhal, P Casaer, et al.American Journal of Medical Genetics. Part A|February 28, 2003
Personality profiles of children and adolescents with neurofibromatosis type 1P Prinzie, M J Descheemaeker, A Vogels, et al.American Journal of Medical Genetics|February 1, 1991
Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytesP B Jacky, Y R Ahuja, K Anyane-Yeboa, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 23, 2006
New models to predict depth of infiltration in endometrial carcinoma based on transvaginal sonographyF De Smet, J De Brabanter, T Van den Bosch, et al.American Journal of Medical Genetics|November 20, 1995
Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literatureC E de Die-Smulders, J J Engelen, C T Schrander-Stumpel, et al.Kidney International|August 3, 2006
Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndromeP Vylet'al, M Kublová, M Kalbácová, 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.European Journal of Human Genetics : EJHG|January 1, 1993
Mental status and fragile X expression in relation to FMR-1 gene mutationB B de Vries, A M Wiegers, E de Graaff, et al.Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.Journal of Medical Genetics|May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomaliesC T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.Pageof 89