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Human Molecular Genetics|September 1, 1994
Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictionsK Petrukhin, S Lutsenko, I Chernov, et al.Journal of Medical Genetics|June 1, 1986
Molecular genetics of human chromosome 4J A Gusella, T C Gilliam, M E MacDonald, et al.Genomics|December 1, 1992
Identification and localization of microsatellite markers covering human chromosome 18K Rojas, R E Straub, A Kurtz, et al.Genomics|January 1, 1993
A microsatellite genetic linkage map of human chromosome 18R E Straub, M C Speer, Y Luo, et al.Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy geneS Selig, S Bruno, J M Scharf, et al.Human Molecular Genetics|August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pJ A Knowles, Y Shugart, P Banerjee, et al.Neurology|April 14, 2004
LGI1 mutations in autosomal dominant partial epilepsy with auditory featuresR Ottman, M R Winawer, S Kalachikov, et al.Annals of Neurology|July 1, 1997
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologuesC H Wang, T A Carter, K Das, et al.Neurology|April 1, 1995
Autosomal dominant distal spinal muscular atrophy in four generationsK B Boylan, D R Cornblath, J D Glass, et al.Genomics|November 1, 1989
Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophreniaT C Gilliam, N B Freimer, C A Kaufmann, et al.Pageof 7