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Clinical Genetics|June 1, 1994
Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocationE Smeets, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1991
The 48,XXYY syndrome. Follow-up data on clinical characteristics and psychological findings in 4 patientsM Borghgraef, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the childD Soekarman, J P Fryns, H van den BergheEuropean Journal of Pediatrics|November 4, 1977
The Greig polysyndactyly-craniofacial dysmorphism syndromeJ P Fryns, W Coeck, H van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndromeM Borghgraef, J P Fryns, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?J P Fryns, A Vogels, H van den BergheClinical Genetics|February 1, 1990
Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A "new" mental retardation syndromeJ P Fryns, A Vogels, H van den BergheHuman Genetics|September 1, 1988
X-chromosome polysomy in the male. The Leuven experience 1966-1987A Kleczkowska, J P Fryns, H Van den BergheClinical Genetics|January 1, 1988
De novo 3q/7q translocation and associated interstitial 7q35 deletionJ P Fryns, A Kleczkowska, H van den BerghePageof 90