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Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.Annales 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 BergheMolecular Syndromology|December 6, 2011
FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in ZebrafishI Balikova, K Devriendt, J-P Fryns, et al.Annales De Genetique|January 1, 1980
Partial distal 12q trisomyA de Muelenaere, J P Fryns, H Van Den BergheClinical 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 BergheClinical Genetics|October 1, 1994
Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14)P Petit, C Hilliker, F Van Leuven, et al.Pageof 89