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Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.Journal of Medical Genetics|October 22, 2003
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13P J Coucke, M W Wessels, P Van Acker, et al.The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Variable regions of chromosome 11 loss in different pathological tissues of a patient with the multiple endocrine neoplasia type I syndromeA Beckers, R Abs, E Reyniers, et al.Proceedings of the National Academy of Sciences of the United States of America|May 13, 1997
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficitsT A Comery, J B Harris, P J Willems, et al.Applied and Environmental Microbiology|December 31, 2014
Population biology of intestinal enterococcus isolates from hospitalized and nonhospitalized individuals in different age groupsAna P Tedim, Patricia Ruiz-Garbajosa, Jukka Corander, et al.Antimicrobial Agents and Chemotherapy|December 25, 2002
Fluconazole susceptibility of vaginal isolates obtained from women with complicated Candida vaginitis: clinical implicationsJ D Sobel, M Zervos, B D Reed, et al.The Analyst|January 21, 2020
COvalent monolayer patterns in Microfluidics by PLasma etching Open Technology - COMPLOTStan B J Willems, Jaccoline Zegers, Anton Bunschoten, et al.Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.European Journal of Biochemistry|November 1, 1994
Characterization of a rat C6 glioma-secreted follistatin-related protein (FRP). Cloning and sequence of the human homologueA Zwijsen, H Blockx, W Van Arnhem, et al.Family Practice|December 10, 2013
Cystitis: antibiotic prescribing, consultation, attitudes and opinionsCarmen S J Willems, Joep van den Broek D'Obrenan, Mattijs E Numans, et al.Pageof 50