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Annales De Genetique|April 6, 2002
Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?Annick Vogels, Maureen Holvoet, Mie-Jef Descheemaeker, et al.International Journal of Paediatric Dentistry|December 19, 2007
The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patientsIsabelle Bailleul-Forestier, Veroniek Verhaeghe, Jean-Pierre Fryns, et al.European Child & Adolescent Psychiatry|December 7, 2002
Psychiatric genetics: the case of single gene disordersJean Steyaert, Jean-Pierre FrynsEuropean Journal of Human Genetics : EJHG|May 21, 2009
Angelman syndrome (AS, MIM 105830)Griet Van Buggenhout, Jean-Pierre FrynsOrphanet Journal of Rare Diseases|July 13, 2006
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)Griet Van Buggenhout, Jean-Pierre FrynsAmerican Journal of Medical Genetics|October 26, 2002
Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnosesIngrid Witters, Philippe Moerman, Jean-Pierre FrynsAnnales De Genetique|September 1, 2004
A familial complex chromosome translocation resulting in duplication of 6p25J R Vermeesch, R Thoelen, Jean Pierre FrynsGenome Medicine|July 31, 2010
Piecing together the problems in diagnosing low-level chromosomal mosaicismCaroline Robberecht, Jean-Pierre Fryns, Joris Robert VermeeschPrenatal Diagnosis|August 10, 2004
Positive maternal serum triple test screening in severe early onset hypophosphatasiaIngrid Witters, Philippe Moerman, Etienne Mornet, et al.Pageof 19