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Clinical Genetics|May 1, 1989
Retinitis pigmentosa, hearing loss and vitiligo: report of two patientsA M Dereymaeker, J P Fryns, J Ars, et al.Human Genetics|January 1, 1985
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritanceM Buttiëns, J P Fryns, P Jonckheere, et al.Human Mutation|January 1, 1996
Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndromeR Wu, E Legius, W Robberecht, et al.Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndromeH Van Esch, P Groenen, J P Fryns, et al.Journal of Medical Genetics|June 3, 1999
X linked mental retardation and infantile spasms in a family: new clinical data and linkage to Xp11.4-Xp22.11P Strømme, K Sundet, C Mørk, et al.European Journal of Pediatrics|September 1, 1980
Multiple synostosis syndromeJ C Pedersen, J P Fryns, G Carpentier, et al.Acta Oto-Rhino-Laryngologica Belgica|March 21, 2001
Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, N Rommel, K Devriendt, et al.Clinical Genetics|January 1, 1992
Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.Clinical Genetics|December 1, 1991
Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndromeL M Curfs, A M Wiegers, J R Sommers, et al.Journal De Genetique Humaine|December 1, 1988
A systematic cytogenetic study of a population of 1170 mentally retarded and/or behaviourly disturbed patients including fragile X-screening. The Hondsberg experienceG A Schreppers-Tijdink, L M Curfs, A Wiegers, et al.Pageof 89