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O Riess

Showing results (11-20 of 144) with videos related to

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Neurogenetics|March 25, 2000
Characterization of the rat spinocerebellar ataxia type 3 geneI Schmitt, T Brattig, M Gossen, et al.
Neurotoxicity Research|April 24, 2003
Iron in neurodegenerative disordersD. Berg, G. Becker, P. Riederer, et al.
Clinical Genetics|August 1, 1989
Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria familiesM Stuhrmann, O Riess, E Mönch, et al.
Biochemical and Biophysical Research Communications|November 30, 1994
Characterization of the gene for human neutrophil-activating peptide 78 (ENA-78)M S Corbett, I Schmitt, O Riess, et al.
Human Genetics|December 1, 1993
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25O Riess, C Epplen, I Siedlaczck, et al.
Electrophoresis|October 1, 1993
Simple repetitive (GAA)n loci in the human genomeI Siedlaczck, C Epplen, O Riess, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the diseaseG Lucotte, N Gérard, P Roubertoux, et al.
Clinical Genetics|October 1, 1987
Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic RepublicO Riess, A Michel, A Speer, et al.
Neurology|December 17, 1998
Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?L Schöls, J Haan, O Riess, et al.
Human Molecular Genetics|September 1, 1993
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's diseaseO Riess, A Noerremoelle, S A Soerensen, et al.
Pageof 15

Showing results (11-20 of 144) with videos related to

Sort By:
Pageof 15
Neurogenetics|March 25, 2000
Characterization of the rat spinocerebellar ataxia type 3 geneI Schmitt, T Brattig, M Gossen, et al.
Neurotoxicity Research|April 24, 2003
Iron in neurodegenerative disordersD. Berg, G. Becker, P. Riederer, et al.
Clinical Genetics|August 1, 1989
Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria familiesM Stuhrmann, O Riess, E Mönch, et al.
Biochemical and Biophysical Research Communications|November 30, 1994
Characterization of the gene for human neutrophil-activating peptide 78 (ENA-78)M S Corbett, I Schmitt, O Riess, et al.
Human Genetics|December 1, 1993
Chromosomal assignment of the human smg GDP dissociation stimulator gene to human chromosome 4q21-q25O Riess, C Epplen, I Siedlaczck, et al.
Electrophoresis|October 1, 1993
Simple repetitive (GAA)n loci in the human genomeI Siedlaczck, C Epplen, O Riess, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the diseaseG Lucotte, N Gérard, P Roubertoux, et al.
Clinical Genetics|October 1, 1987
Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic RepublicO Riess, A Michel, A Speer, et al.
Neurology|December 17, 1998
Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?L Schöls, J Haan, O Riess, et al.
Human Molecular Genetics|September 1, 1993
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's diseaseO Riess, A Noerremoelle, S A Soerensen, et al.
Pageof 15