Showing results (281-290 of 883) with videos related to
Sort By:
Pageof 89
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
13q deletion syndrome in an adult mentally retarded patientG Van Buggenhout, J Trommelen, B Hamel, et al.Clinical Dysmorphology|August 24, 1999
Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Segmentary fibrous dysplasia manifesting as macrodactylyK Keymolen, L De Smet, H Kenis, et al.Human Genetics|April 1, 1997
Homozygosity by descent for a COL1A2 mutation in two sibs with severe osteogenesis imperfecta and mild clinical expression in the heterozygotesA De Paepe, L Nuytinck, M Raes, et al.American Journal of Medical Genetics|July 15, 1992
A severe case of mandibuloacral dysplasia in a girlC Schrander-Stumpel, A Spaepen, J P Fryns, et al.Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Mandibulo-acral dysplasia in a one-year-old boyG Vantrappen, L Feenstra, C Macours-Verelst, et al.Clinical Genetics|December 1, 1993
Cowden syndrome: report of a large family with macrocephaly and increased severity of signs in subsequent generationsA M Hanssen, H Werquin, E Suys, et al.European Journal of Pediatrics|May 1, 1981
The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a familyJ P Fryns, G Van Noyen, H Van den BergheClinical 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 HamersPageof 89