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European Journal of Human Genetics : EJHG|October 22, 1998
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large familyE Legius, E Schollen, G Matthijs, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31)G Van Buggenhout, P H Moerman, J P FrynsJournal De Genetique Humaine|March 1, 1980
Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndromeP Goddeeris, J P Fryns, H van den BergheAnnales De Genetique|January 1, 1986
47,XXY karyotype in a patient with Beckwith-Wiedemann syndromeJ P Fryns, A Kleczkowska, H Van den BergheAnnales De Genetique|January 1, 1990
Interstitial deletion of the short arm of chromosome 12. Report of a new patient and review of the literatureJ P Fryns, A Kleczkowska, H Van den BergheClinical Genetics|December 1, 1991
Cohen syndrome: fertility in a female patientJ P Fryns, F Lemmens, H van den BergheClinical Genetics|September 1, 1995
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" associationJ P Fryns, E Smeets, H Van den BergheEuropean Journal of Obstetrics, Gynecology, and Reproductive Biology|April 16, 1991
Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetusP Petit, D Thomas, P Moerman, et al.Clinical Genetics|October 1, 1984
The Coffin-Siris syndrome: report of a family and further delineationM Haspeslagh, J P Fryns, H van den BergheJournal De Genetique Humaine|June 1, 1982
Robertsonian t(Dq;Dq) translocations in manJ P Fryns, A Kleczkowska, H Van den BerguePageof 90