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Genetic Counseling (Geneva, Switzerland)|May 23, 2012
A new syndrome: multiple congenital abnormalities and mental retardation in two brothersM Dundar, S Y Ozdemir, J P FrynsAmerican Journal of Medical Genetics|May 15, 1994
Regional Proteus syndrome and somatic mosaicismE Smeets, J P Fryns, M M CohenEuropean Journal of Pediatrics|December 1, 1992
Deletion of the short arm of the X chromosome: a hereditary form of Turner syndromeG Massa, M Vanderschueren-Lodeweyckx, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 16, 2004
Bilateral aplasia of the thumb, proximal radioulnar synostosis and unilateral synostosis of metacarpals 4 and 5Ph Debeer, L De Smet, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 29, 1998
Symbrachydactyly involving hands and feetL De Smet, G Fabry, J P FrynsGenetic Counseling (Geneva, Switzerland)|April 23, 2005
De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literatureT Lukusa, J R Vermeesch, J P FrynsJournal of Mental Deficiency Research|June 1, 1991
The partial monosomy 10q syndrome: report on two patients and review of the developmental dataC Schrander-Stumpel, J P Fryns, G HamersGenetic Counseling (Geneva, Switzerland)|January 1, 1996
A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?G van Buggenhout, P Decock, J P FrynsInternational Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|December 14, 2005
Report of an unusual problematic uterine smooth muscle neoplasm, emphasizing the prognostic importance of coagulative tumor cell necrosisF Amant, P Moerman, I VergotePageof 89