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Annales De Genetique|January 1, 1989
Interstitial deletion of the short arm of chromosome 4. A phenotype distinct from the Wolf-Hirschhorn syndromeJ P Fryns, Yang-Aisheng, A Kleczkowska, et al.Annales De Genetique|January 1, 1986
The fetal phenotype in 2p trisomyJ P Fryns, A Kleczkowska, F Moerman, et al.Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Oculo-auriculo-vertebral spectrum in Klinefelter syndromeL Garavelli, R Virdis, A Donadio, et al.Clinical Genetics|November 1, 1977
Short stature, craniofacial dysmorphism and dento-skeletal abnormalities in a large kindred. A variant of K.B.G. syndrome or a new mental retardation syndromeC Parloir, J P Fryns, J Deroover, et al.Human Genetics|January 1, 1980
Perinatal mortality and XY/XX mosaicism. Report of two patientsJ P Fryns, M Haspeslagh, E Vandenbussche, et al.Journal of Medical Genetics|April 1, 1993
Profound mental retardation, characteristic facies with midfacial hypoplasia and premature frontotemporal balding, muscular hypotrophy, and small patellae in two unrelated male patientsJ P Fryns, P Thiry, J Geutjens, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.American Journal of Medical Genetics|September 1, 1991
Apparent late-onset Cockayne syndrome and interstitial deletion of the long arm of chromosome 10 (del(10)(q11.23q21.2))J P Fryns, J Bulcke, P Verdu, et al.Clinical Genetics|April 1, 1994
Prader-Willi-like phenotype in fragile X syndromeC Schrander-Stumpel, W J Gerver, H Meyer, et al.American Journal of Medical Genetics|December 1, 1990
Opitz C syndrome and pseudohypoaldosteronismJ De Koster, E Legius, F de Zegher, et al.Pageof 89