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S E Ide

Showing results (1-10 of 17) with videos related to

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Cancer Genetics and Cytogenetics|November 1, 1996
Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22M H Polymeropoulos, S E Ide, K Becker, et al.
Human Molecular Genetics|July 1, 1993
Dinucleotide repeat polymorphism at the D11S982E locusH Xiao, S E Ide, C R Merril, et al.
Genomics|November 15, 1996
Brachydactyly type C gene maps to human chromsome 12q24M H Polymeropoulos, S E Ide, T Magyari, et al.
Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism at the D14S99E locusM H Polymeropoulos, H Xiao, S E Ide, et al.
Clinical Biochemistry|February 1, 1997
Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiencyJ J Higgins, S E Ide, J S Oghalai, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|November 26, 1999
Genomic structure and localization of the human protein phosphatase 2A BRgamma regulatory subunitR Torres, S E Ide, A Dehejia, et al.
Human Genetics|November 1, 1996
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the AmishS E Ide, R I Ortiz de Luna, C A Francomano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Evidence for a new spinocerebellar ataxia locusJ J Higgins, L T Pho, S E Ide, et al.
Nature Genetics|June 1, 1995
The gene for pycnodysostosis maps to human chromosome 1cen-q21M H Polymeropoulos, R I Ortiz De Luna, S E Ide, et al.
Neurology|January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph diseaseJ J Higgins, L E Nee, O Vasconcelos, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Cancer Genetics and Cytogenetics|November 1, 1996
Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22M H Polymeropoulos, S E Ide, K Becker, et al.
Human Molecular Genetics|July 1, 1993
Dinucleotide repeat polymorphism at the D11S982E locusH Xiao, S E Ide, C R Merril, et al.
Genomics|November 15, 1996
Brachydactyly type C gene maps to human chromsome 12q24M H Polymeropoulos, S E Ide, T Magyari, et al.
Human Molecular Genetics|April 1, 1993
Dinucleotide repeat polymorphism at the D14S99E locusM H Polymeropoulos, H Xiao, S E Ide, et al.
Clinical Biochemistry|February 1, 1997
Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiencyJ J Higgins, S E Ide, J S Oghalai, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|November 26, 1999
Genomic structure and localization of the human protein phosphatase 2A BRgamma regulatory subunitR Torres, S E Ide, A Dehejia, et al.
Human Genetics|November 1, 1996
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the AmishS E Ide, R I Ortiz de Luna, C A Francomano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Evidence for a new spinocerebellar ataxia locusJ J Higgins, L T Pho, S E Ide, et al.
Nature Genetics|June 1, 1995
The gene for pycnodysostosis maps to human chromosome 1cen-q21M H Polymeropoulos, R I Ortiz De Luna, S E Ide, et al.
Neurology|January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph diseaseJ J Higgins, L E Nee, O Vasconcelos, et al.
Pageof 2