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Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Minimal dysmorphic stigmata in 9q deletion of paternal originA Kleczkowska, J P Fryns, L Lemli, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypesP Petit, K Devriendt, M Azou, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Progressive pseudorheumatoid dysplasia: report of a patient with symptoms present at birthG van Buggenhout, L De Smet, P Maroteaux, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32A Kleczkowska, J P Fryns, P Lemay, et al.Annales De Genetique|February 16, 2000
Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosomeT Lukusa, L van den Berghe, E Smeets, et al.Clinical Dysmorphology|October 25, 2000
A young female with asymmetric manifestations of larsen syndrome: another example of unilateral somatic cell-line mosaicismS G Frints, L De Smet, G Fabry, et al.Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.Clinical Genetics|May 1, 1993
The hand-foot-genital syndrome: on the variable expression in affected malesJ P Fryns, A Vogels, P Decock, et al.Clinical Genetics|February 1, 1984
The psychological profile of the fragile X syndromeJ P Fryns, J Jacobs, A Kleczkowska, et al.Clinical Genetics|September 1, 1993
MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplicationJ P Fryns, M Borghgraef, F Lemmens, et al.Pageof 89