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American Journal of Medical Genetics|January 1, 1993
Apparent Greig cephalopolysyndactyly and sinus node diseaseJ P Fryns, P De Waele, L Van der Hauwaert, et al.Human Genetics|September 1, 1991
"Spontaneous" FRA16B is a hot spot for sister chromatid exchangesT Lukusa, E Meulepas, J P Fryns, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1984
Antenatal ultrasound diagnosis of fetal malformations: possibilities, limitations and dilemmasK Vandenberghe, F De Wolf, J P Fryns, et al.Journal of Intellectual Disability Research : JIDR|September 12, 2007
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an updateB De Smedt, K Devriendt, J-P Fryns, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|May 1, 1990
The lethal multiple pterygium syndrome: prenatal ultrasonographic and postmortem findings; a case reportC E de Die-Smulders, H J Vonsée, J A Zandvoort, et al.Dermatology (Basel, Switzerland)|February 14, 2012
Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29E Chabchoub, O Cogulu, B Durmaz, et al.Clinical Dysmorphology|May 29, 2000
Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphismK Devriendt, K Keymolen, L Roelen, et al.Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 1, 1990
Holoprosencephaly and postaxial polydactyly with normal chromosomes. Another observation of a new malformation syndrome; a case reportP R Ramaekers, E Legius, A Verloes, et al.Pageof 89