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European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|February 23, 2011
Quantitative analysis of the anterolateral ossification mass in diffuse idiopathic skeletal hyperostosis of the thoracic spineJ J Verlaan, L A Westerveld, J W van Keulen, et al.Biochemical and Biophysical Research Communications|May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersS Brul, E A Wiemer, A Westerveld, et al.Human Genetics|June 1, 1996
Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locusH Caron, P van Sluis, R Buschman, et al.Human Genetics|January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodiesR A Barneveld, W Keijzer, F P Tegelaers, et al.Medical and Pediatric Oncology|November 1, 1996
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumorsM Mannens, M Alders, B Redeker, et al.European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.Cytogenetics and Cell Genetics|May 27, 1999
Integrated genetic and physical map of the 1q31-->q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenesS van Soest, M J van Rossem, J R Heckenlively, et al.Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragmentsJ M Hoovers, L M Kalikin, L A Johnson, et al.Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.Pageof 11