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The Journal of Biological Chemistry|October 14, 1994
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promotersU Suter, G J Snipes, R Schoener-Scott, et al.American Journal of Human Genetics|November 1, 1988
Identification of a mutation in the structural alpha-L-fucosidase gene in fucosidosisP J Willems, J K Darby, R A DiCioccio, et al.The New England Journal of Medicine|July 8, 1993
Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 geneB B Roa, C A Garcia, U Suter, et al.Nature Genetics|October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, L Pentao, et al.Nature Genetics|June 1, 1992
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1AP I Patel, B B Roa, A A Welcher, et al.Neurology|April 6, 2000
Combined assessment of tau and neuronal thread protein in Alzheimer's disease CSFP J Kahle, M Jakowec, S J Teipel, et al.Pageof 18