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Genomics|August 1, 1989
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21M K McCormick, A Schinzel, M B Petersen, 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.Cell|February 22, 1991
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndromeM V Bell, M C Hirst, Y Nakahori, et al.Journal of the Neurological Sciences|May 20, 1998
Machado-Joseph disease in three Scandinavian familiesT Løkkegaard, J E Nielsen, L Hasholt, et al.European Journal of Human Genetics : EJHG|August 22, 2000
Founder effect in spinal and bulbar muscular atrophy (SBMA) in ScandinaviaA Lund, B Udd, V Juvonen, et al.Nature Genetics|October 1, 1996
A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindnessH Jin, M May, L Tranebjaerg, et al.Ophthalmic Genetics|January 23, 2002
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a geneL Tranebjaerg, P K Jensen, M Van Ghelue, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 14, 2007
Persistent strains of coagulase-negative staphylococci in a neonatal intensive care unit: virulence factors and invasivenessC Klingenberg, A Rønnestad, A S Anderson, et al.American Journal of Nephrology|March 29, 2019
Canagliflozin Prevents Intrarenal Angiotensinogen Augmentation and Mitigates Kidney Injury and Hypertension in Mouse Model of Type 2 Diabetes MellitusT Cooper Woods, Ryousuke Satou, Kayoko Miyata, et al.American Journal of Human Genetics|April 16, 1998
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13P Pekkarinen, I Hovatta, P Hakola, et al.Pageof 11