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N Tayebi

Showing results (1-10 of 31) with videos related to

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American Journal of Human Genetics|September 1, 1996
Differentiation of the glucocerebrosidase gene from pseudogene by long-template PCR: implications for Gaucher diseaseN Tayebi, S Cushner, E Sidransky
American Journal of Medical Genetics|November 20, 1995
Congenital ichthyosis preceding neurologic symptoms in two sibs with type 2 Gaucher diseaseA Fujimoto, N Tayebi, E Sidransky
Clinical Pediatrics|July 1, 1995
Diagnosing Gaucher disease. Early recognition, implications for treatment, and genetic counselingE Sidransky, N Tayebi, E I Ginns
Molecular Genetics and Metabolism|October 21, 1999
Type 2 gaucher disease: an expanding phenotypeN Tayebi, D L Stone, E Sidransky
Human Genetics|December 29, 2000
Gene rearranagement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion geneN Tayebi, J Park, V Madike, et al.
Biochemical 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.
American Journal of Medical Genetics|December 18, 1996
55-base pair deletion in certain patients with Gaucher disease complicates screening for common Gaucher allelesN Tayebi, H Stern, I Dymarskaia, et al.
Journal of Medical Genetics|November 10, 2000
Cardiovascular fibrosis, hydrocephalus, ophthalmoplegia, and visceral involvement in an American child with Gaucher diseaseD L Stone, N Tayebi, C Coble, et al.
Blood Cells, Molecules & Diseases|October 1, 2010
Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneityN Gupta, I M Oppenheim, E F Kauvar, et al.
Human Mutation|January 29, 2000
Glucocerebrosidase gene mutations in patients with type 2 Gaucher diseaseD L Stone, N Tayebi, E Orvisky, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|September 1, 1996
Differentiation of the glucocerebrosidase gene from pseudogene by long-template PCR: implications for Gaucher diseaseN Tayebi, S Cushner, E Sidransky
American Journal of Medical Genetics|November 20, 1995
Congenital ichthyosis preceding neurologic symptoms in two sibs with type 2 Gaucher diseaseA Fujimoto, N Tayebi, E Sidransky
Clinical Pediatrics|July 1, 1995
Diagnosing Gaucher disease. Early recognition, implications for treatment, and genetic counselingE Sidransky, N Tayebi, E I Ginns
Molecular Genetics and Metabolism|October 21, 1999
Type 2 gaucher disease: an expanding phenotypeN Tayebi, D L Stone, E Sidransky
Human Genetics|December 29, 2000
Gene rearranagement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion geneN Tayebi, J Park, V Madike, et al.
Biochemical 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.
American Journal of Medical Genetics|December 18, 1996
55-base pair deletion in certain patients with Gaucher disease complicates screening for common Gaucher allelesN Tayebi, H Stern, I Dymarskaia, et al.
Journal of Medical Genetics|November 10, 2000
Cardiovascular fibrosis, hydrocephalus, ophthalmoplegia, and visceral involvement in an American child with Gaucher diseaseD L Stone, N Tayebi, C Coble, et al.
Blood Cells, Molecules & Diseases|October 1, 2010
Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneityN Gupta, I M Oppenheim, E F Kauvar, et al.
Human Mutation|January 29, 2000
Glucocerebrosidase gene mutations in patients with type 2 Gaucher diseaseD L Stone, N Tayebi, E Orvisky, et al.
Pageof 4