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Clinical Genetics|June 1, 1987
The Brachmann-de Lange syndrome in two siblings of normal parentsJ P Fryns, A M Dereymaeker, M Hoefnagels, et al.American Journal of Medical Genetics|March 4, 2000
Cri du chat syndrome: changing phenotype in older patientsG J Van Buggenhout, E Pijkels, M Holvoet, et al.Genetic Counseling (Geneva, Switzerland)|November 5, 1999
A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardationM Tabaku, E Legius, W Robberecht, et al.Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.Cancer Genetics and Cytogenetics|July 15, 1996
Thymoma with a t(15;22)(p11;q11)P Dal Cin, C De Wolf-Peeters, G Deneffe, et al.Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Cognitive correlates of mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Type III syndactyly and oculodentodigital dysplasia: a clinical spectrumC T Schrander-Stumpel, J B De Groot-Wijnands, C De Die-Smulders, et al.Human Genetics|November 1, 1989
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome. Construction of a mouse-human hybrid cell line containing an i(12p) as the sole human chromosomeJ Zhang, P Marynen, K Devriendt, et al.Clinical Genetics|December 1, 1986
Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formationA Kleczkowska, J P Fryns, M Buttiens, et al.Pageof 89