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Human Genetics|November 16, 1978
Unusual in vivo rearrangements of the Y chromosome with mitotic instability in vitroJ P Fryns, J J Cassiman, H Van den BergheClinical Genetics|April 19, 2011
Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineatedE Chabchoub, D Willekens, J R Vermeesch, et al.Genetic Counseling (Geneva, Switzerland)|July 28, 1999
13q deletion syndrome in an adult mentally retarded patientG Van Buggenhout, J Trommelen, B Hamel, 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)|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 BerghePediatrics|April 1, 1984
Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasiaP Moerman, J P Fryns, P Goddeeris, et al.Pageof 90