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Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Martin-Bell phenotype in males with acquired central nervous system lesions. 15 males diagnosed during a systematic etiological study of 274 mentally retarded malesJ P Fryns, P Volcke, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1992
The cardio-facio-cutaneous (CFC) syndrome: autosomal dominant inheritance in a large familyJ P Fryns, P Volcke, H Van den BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1996
Nager acrofacial dysostosis. An adult male with severe neurological deficitJ P Fryns, A Bonhomme, H Van den BergheClinical Genetics|May 1, 1990
Dominant branchial cleft syndrome with characteristics of both branchio-oto-renal and branchio-oculo-facial syndromeE Legius, J P Fryns, H Van den BergheThe Journal of Rheumatology|May 1, 1994
A familial syndrome of dwarfism, bilateral club feet, premature aging and progressive panhypogammaglobulinemiaJ Lenaerts, J P Fryns, R Westhovens, et al.Journal of Medical Genetics|September 1, 1992
Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardationJ P Fryns, J Delooz, H Van Den BergheGenetic Counseling (Geneva, Switzerland)|July 28, 1999
Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotypeE Goossens, P Decock, S Potgieter, et al.Clinical Genetics|December 1, 1989
An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformationM Buttiens, J P Fryns, H van den BergheAmerican Journal of Medical Genetics|August 1, 1989
Cardio-facio-cutaneous (CFC) syndrome: report of a new patientK Chrzanowska, J P Fryns, H Van den BerghePageof 89