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Clinical Genetics|September 1, 1995
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" associationJ P Fryns, E Smeets, H Van den BergheClinical 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 BergueAmerican Journal of Medical Genetics|August 9, 1996
Fragile X mutation and FG syndrome-like phenotypeC Piussan, M Mathieu, P Berquin, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
The Floating-Harbor syndrome: report of another patient and differential diagnosis with Shprintzen syndromeE Smeets, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1995
Severe axial mesodermal dysplasia spectrum in an infant of a diabetic motherM Depraetere, R Dehauwere, P Mariën, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 1, 1989
X-to-X translocation associated with gonadal dysgenesis and discrete Turner syndrome stigmata; a case reportA Kleczkowska, J P Fryns, H Van den BergheAnnales De Genetique|January 1, 1992
Trisomy of the short arm of chromosome 4: the changing phenotype with ageA Kleczkowska, J P Fryns, H van den BergheClinical Genetics|December 1, 1992
Posterior scalp defects in Opitz syndrome. Another symptom related to a defect in midline developmentJ P Fryns, J Delooz, H van den BergheEuropean Journal of Pediatrics|October 1, 1983
Familial infantile cortical hyperostosisL Emmery, J Timmermans, J Christens, et al.Pageof 89