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Cytogenetics and Cell Genetics|January 1, 1994
Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24M S Malo, B J Blanchard, J M Andresen, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndromeR A Norris, K K Scott, C S Moore, et al.The Journal of Biological Chemistry|May 6, 1994
Complete cDNA sequence of a human dioxin-inducible mRNA identifies a new gene subfamily of cytochrome P450 that maps to chromosome 2T R Sutter, Y M Tang, C L Hayes, et al.Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.American Journal of Medical Genetics|August 1, 1993
Family with 22-derived marker chromosome and late-onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high-level repeat sequences using fluorescence in situ hybridizationM E Percy, T G Dearie, E W Jabs, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1993
Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humansP Gregor, R H Reeves, E W Jabs, et al.American Journal of Medical Genetics|June 28, 2001
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3D N Schweitzer, J M Graham, R S Lachman, et al.Genomics|September 1, 1991
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this regionE W Jabs, C A Coss, S J Hayflick, et al.American Journal of Human Genetics|May 20, 1999
A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafnessM J Kovach, J P Lin, S Boyadjiev, et al.Pageof 11