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American Journal of Human Genetics|October 1, 1987
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunctionG Annerén, M Andersson, D C Page, et al.Acta Paediatrica Scandinavica|March 1, 1978
The incidence of diabetes mellitus in Swedish children 1970--1975G Sterky, G Holmgren, K H Gustavson, et al.Genomics|December 1, 1994
Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 lociC Graff, K Forsman, C Larsson, et al.Prenatal Diagnosis|August 1, 1991
Early prenatal diagnosis of the fragile site at Xq27.3 associated with Martin-Bell syndromeN Tommerup, F Søndergaard, A Hanauer, et al.American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.Human Mutation|November 26, 1998
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndromeA Sillén, I Anton-Lamprecht, C Braun-Quentin, et al.Human Mutation|April 29, 1998
Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma geneP Höglund, S Haila, K H Gustavson, et al.The Journal of Pediatrics|August 1, 1989
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleW B Rizzo, A L Dammann, D A Craft, et al.Journal of Medical Genetics|February 1, 1993
Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor geneF M Richards, E R Maher, F Latif, et al.Experimental and Clinical Immunogenetics|January 1, 1995
Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatelliteD Agardi, M Pigg, A G Sjöholm, et al.Pageof 14