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Gene|December 15, 1990
Prevalent and rare mutations among Gaucher patientsN Eyal, S Wilder, M HorowitzHuman Genetics|July 1, 1991
Three unique base pair changes in a family with Gaucher diseaseN Eyal, N Firon, S Wilder, et al.Developmental Neuroscience|January 1, 1991
Molecular aspects of Gaucher diseaseH Levy, A Or, N Eyal, et al.DNA (Mary Ann Liebert, Inc.)|April 1, 1987
Efficient in vitro and in vivo expression of human glucocerebrosidase cDNAO Reiner, S Wilder, D Givol, et al.American Journal of Human Genetics|March 1, 1990
Genotype assignment in Gaucher disease by selective amplification of the active glucocerebrosidase geneN Firon, N Eyal, E H Kolodny, et al.American Journal of Medical Genetics|August 1, 1990
Mutation analysis of an Ashkenazi Jewish family with Gaucher disease in three successive generationsE H Kolodny, N Firon, N Eyal, et al.European Journal of Human Genetics : EJHG|January 15, 1999
A benign polymorphism in the aspartoacylase gene may cause misinterpretation of Canavan gene testingO Propheta, N Magal, M Shohat, et al.Genomics|January 1, 1989
The human glucocerebrosidase gene and pseudogene: structure and evolutionM Horowitz, S Wilder, Z Horowitz, et al.American Journal of Human Genetics|March 1, 1989
Characterization of mutations in Gaucher patients by cDNA cloningM Wigderson, N Firon, Z Horowitz, et al.Vital and Health Statistics. Series 10, Data From the National Health Survey|August 29, 2014
Acute conditions incidence and associated disability, United States - july 1968-june 1969C S WilderPageof 184