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American Journal of Medical Genetics|March 15, 1994
Progress in a genome scan for linkage in schizophrenia in a large Swedish kindredC L Barr, J L Kennedy, A J Pakstis, et al.Human Genetics|July 8, 1999
The mutation spectrum of the bestrophin protein--functional implicationsB Bakall, T Marknell, S Ingvast, et al.Clinical Genetics|July 1, 1992
Linkage analysis in properdin deficiency families: refined location in proximal XpC Wadelius, M Pigg, M Sundvall, et al.Experimental Eye Research|May 5, 2007
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)B Bakall, R A Radu, J B Stanton, et al.Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.Human Genetics|August 24, 1999
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathiesR Allikmets, J M Seddon, P S Bernstein, et al.Neurology|December 17, 1998
Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14B A Neubauer, B Fiedler, B Himmelein, et al.Nature Genetics|July 14, 1998
Identification of the gene responsible for Best macular dystrophyK Petrukhin, M J Koisti, B Bakall, et al.Pageof 5