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O Riess

Showing results (61-70 of 144) with videos related to

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American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Human Genetics|January 1, 1991
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuriaJ Jaruzelska, K F Henriksen, F Güttler, et al.
Journal of Neural Transmission. Supplementum|October 5, 2006
Genetic causes of Parkinson's disease: extending the pathwayO Riess, R Krüger, H Hochstrasser, et al.
Human Molecular Genetics|July 1, 1995
Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during developmentI Schmitt, D Bächner, D Megow, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 31, 2002
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patientsP Wintermeyer, O Riess, L Schöls, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Clinical Genetics|June 1, 1986
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLPA Speer, H H Dahl, O Riess, et al.
Archives of Neurology|October 13, 2000
Extrapyramidal motor signs in degenerative ataxiasL Schöls, S Peters, S Szymanski, et al.
Human Genetics|February 1, 1995
Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's diseaseG Lucotte, J C Turpin, O Riess, et al.
Molecular Syndromology|January 18, 2013
Mirror-image asymmetry in monozygotic twins with kabuki syndromeA Riess, A Dufke, O Riess, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Human Genetics|January 1, 1991
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuriaJ Jaruzelska, K F Henriksen, F Güttler, et al.
Journal of Neural Transmission. Supplementum|October 5, 2006
Genetic causes of Parkinson's disease: extending the pathwayO Riess, R Krüger, H Hochstrasser, et al.
Human Molecular Genetics|July 1, 1995
Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during developmentI Schmitt, D Bächner, D Megow, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 31, 2002
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patientsP Wintermeyer, O Riess, L Schöls, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Clinical Genetics|June 1, 1986
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLPA Speer, H H Dahl, O Riess, et al.
Archives of Neurology|October 13, 2000
Extrapyramidal motor signs in degenerative ataxiasL Schöls, S Peters, S Szymanski, et al.
Human Genetics|February 1, 1995
Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's diseaseG Lucotte, J C Turpin, O Riess, et al.
Molecular Syndromology|January 18, 2013
Mirror-image asymmetry in monozygotic twins with kabuki syndromeA Riess, A Dufke, O Riess, et al.
Pageof 15