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B K Stubblefield

Showing results (1-10 of 16) with videos related to

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Nucleic Acids Research|August 11, 1988
Human tyrosine hydroxylase (TH) genomic fragment (pHGTH4) identifies a PstI polymorphismJ R Kelsoe, B K Stubblefield, E I Ginns
Clinical Genetics|May 23, 2009
Glucocerebrosidase mutation H255Q appears to be exclusively in cis with D409H: structural implicationsJ Vithayathil, G Gibney, A D Baxevanis, et al.
Clinical Genetics|January 1, 1992
Gaucher patients with oculomotor abnormalities do not have a unique genotypeE Sidransky, S Tsuji, B K Stubblefield, et al.
Journal of Neurochemistry|November 1, 1988
Regional distribution of the GABAA/benzodiazepine receptor (alpha subunit) mRNA in rat brainP Montpied, B M Martin, S L Cottingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1988
Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individualsS Tsuji, B M Martin, J A Barranger, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
Analytical Biochemistry|March 1, 1995
Direct sequencing of trinucleotide repeats from cosmid genomic DNA templateR A Philibert, G A Hawkins, P Damschroder-Williams, et al.
Journal of Medical Genetics|June 7, 2005
Divergent phenotypes in Gaucher disease implicate the role of modifiersO Goker-Alpan, K S Hruska, E Orvisky, et al.
Clinical Genetics|March 21, 2002
The E326K mutation and Gaucher disease: mutation or polymorphism?J K Park, N Tayebi, B K Stubblefield, et al.
Pediatric Research|May 19, 1998
Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's diseaseN Tayebi, K J Reissner, E K Lau, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|August 11, 1988
Human tyrosine hydroxylase (TH) genomic fragment (pHGTH4) identifies a PstI polymorphismJ R Kelsoe, B K Stubblefield, E I Ginns
Clinical Genetics|May 23, 2009
Glucocerebrosidase mutation H255Q appears to be exclusively in cis with D409H: structural implicationsJ Vithayathil, G Gibney, A D Baxevanis, et al.
Clinical Genetics|January 1, 1992
Gaucher patients with oculomotor abnormalities do not have a unique genotypeE Sidransky, S Tsuji, B K Stubblefield, et al.
Journal of Neurochemistry|November 1, 1988
Regional distribution of the GABAA/benzodiazepine receptor (alpha subunit) mRNA in rat brainP Montpied, B M Martin, S L Cottingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1988
Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individualsS Tsuji, B M Martin, J A Barranger, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
Analytical Biochemistry|March 1, 1995
Direct sequencing of trinucleotide repeats from cosmid genomic DNA templateR A Philibert, G A Hawkins, P Damschroder-Williams, et al.
Journal of Medical Genetics|June 7, 2005
Divergent phenotypes in Gaucher disease implicate the role of modifiersO Goker-Alpan, K S Hruska, E Orvisky, et al.
Clinical Genetics|March 21, 2002
The E326K mutation and Gaucher disease: mutation or polymorphism?J K Park, N Tayebi, B K Stubblefield, et al.
Pediatric Research|May 19, 1998
Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's diseaseN Tayebi, K J Reissner, E K Lau, et al.
Pageof 2