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Clinical Genetics|March 1, 1990
Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21))C T Schrander-Stumpel, J P Fryns, G G HamersAnnales De Genetique|January 1, 1981
Familial partial distal 18q (18q22-18q23) trisomyA De Muelenaere, J P Fryns, H Van den BergheGenetic Counseling (Geneva, Switzerland)|October 20, 1998
Björnstad syndrome in a patient with mental retardationG Van Buggenhout, J Trommelen, B Hamel, et al.Annales De Genetique|January 1, 1996
Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome?A Vogels, M E Lorenzetti, P Gillis, et al.Human Genetics|October 1, 1979
Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmataJ P Fryns, P De Waele, H Van Den BergheThe Journal of Pediatrics|August 1, 1983
Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophyP Moerman, J P Fryns, P Goddeeris, et al.Annales De Genetique|January 1, 1980
Partial distal 12q trisomyA de Muelenaere, J P Fryns, H Van Den BerghePediatric Pathology|January 1, 1985
Primitive neuroectodermal tumor: a newly recognized cause of early fetal deathP Moerman, P Goddeeris, J P Fryns, et al.Clinical Genetics|June 1, 1993
Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndromeD M Ioan, V Belengeanu, C Maximilian, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Hypomelanosis of Ito and severe sensorineural deafnessJ P Fryns, A M Dereymaeker, H Van Den BerghePageof 90