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American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.Clinical Genetics|April 1, 1996
De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopeniaE Legius, I Wlodarska, L Selleri, et al.Clinical Genetics|April 1, 1986
The Borjeson-Forssman-Lehmann syndrome. A family studyA M Dereymaeker, J P Fryns, M Hoefnagels, et al.Acta Orthopaedica Belgica|August 3, 2002
Genes and orthopedics: from gene to clinic and vice versaPh Debeer, L De Smet, W J M Van De Ven, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years)A Swillen, J P Fryns, A Kleczkowska, et al.Human Genetics|January 1, 1981
Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiencyJ P Fryns, M Azou, J Jaeken, et al.Facts, Views & Vision in Obgyn|April 23, 2014
Trisomy 13, 18, 21, Triploidy and Turner syndrome: the 5T's. Look at the handsG Witters, J Van Robays, C Willekes, et al.European Journal of Pediatrics|March 1, 1981
Aniridia-Wilms' tumor association and 11p interstitial deletionJ P Fryns, J Beirinckx, E De Sutter, et al.American Journal of Medical Genetics|April 1, 1992
MASA syndrome: delineation of the clinical spectrum at prepubertal ageJ P Fryns, C Schrander-Stumpel, C De Die-Smulders, et al.Pageof 89