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Bailliere'S Clinical Haematology|March 14, 1998
Gaucher's disease: the best laid schemes of mice and menE Sidransky, E I GinnsJournal of Genetic Counseling|November 16, 2013
Phenotypic and genotypic heterogeneity in gaucher disease: Implications for genetic counselingE Sidransky, E I GinnsAmerican Journal of Medical Genetics|February 1, 1992
DNA mutation analysis of Gaucher patientsE Sidransky, S Tsuji, B M Martin, et al.Genome Research|October 23, 1997
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher diseaseS L Winfield, N Tayebi, B M Martin, et al.Clinical Pediatrics|July 1, 1995
Diagnosing Gaucher disease. Early recognition, implications for treatment, and genetic counselingE Sidransky, N Tayebi, E I GinnsPediatric Research|October 1, 1992
Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase geneE Sidransky, D M Sherer, E I GinnsBiochemical and Molecular Medicine|April 1, 1996
Genotype D399N/R463C in a patient with type 3 Gaucher disease previously assigned genotype N370S/R463CN Tayebi, J Herman, E I Ginns, et al.Human Mutation|January 1, 1994
DNA mutational analysis of type 1 and type 3 Gaucher patients: how well do mutations predict phenotype?E Sidransky, A Bottler, B Stubblefield, et al.American Journal of Hematology|May 18, 2000
Life-threatening splenic hemorrhage in two patients with Gaucher diseaseD L Stone, E I Ginns, D Krasnewich, et al.Pediatric Research|August 6, 2000
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestationE Orvisky, E Sidransky, C E McKinney, et al.Pageof 26