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Journal of Medical Genetics
|
March 1, 1997
Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene
C Holzmann, A M Saecker, J T Epplen, et al.
Human Molecular Genetics
|
June 1, 1993
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease
O Riess, A Noerremoelle, S A Soerensen, et al.
Neurogenetics
|
December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player
K Häbig, M Walter, S Poths, et al.
Human Molecular Genetics
|
December 1, 1993
Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene
C Zühlke, O Riess, B Bockel, et al.
Acta Biochimica Polonica
|
January 1, 1989
Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria
J Jaruzelska, K Borski, O Riess, et al.
Casopis Lekaru Ceskych
|
February 15, 1995
Molecular genetics of inherited diseases involving human chromosome 4
O Riess, H Schulz, T Träger, et al.
Brain Research. Molecular Brain Research
|
August 3, 2001
Functional characterization of the human Huntington's disease gene promoter
C Holzmann, T Schmidt, G Thiel, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
February 23, 2008
Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity
M Bonin, F P Marx, S Kautzmann, et al.
Genomics
|
December 1, 1991
Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene
B Weber, C Collins, D Kowbel, et al.
Human Genetics
|
February 1, 1997
Transmission distortion of the mutant alleles in spinocerebellar ataxia
O Riess, J T Epplen, G Amoiridis, et al.
Page
of 15
Search research articles
Search
Showing results (21-30 of 144) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
March 1, 1997
Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene
C Holzmann, A M Saecker, J T Epplen, et al.
Human Molecular Genetics
|
June 1, 1993
Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease
O Riess, A Noerremoelle, S A Soerensen, et al.
Neurogenetics
|
December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player
K Häbig, M Walter, S Poths, et al.
Human Molecular Genetics
|
December 1, 1993
Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene
C Zühlke, O Riess, B Bockel, et al.
Acta Biochimica Polonica
|
January 1, 1989
Haplotype analysis of phenylalanine hydroxylase alleles in polish families with phenylketonuria
J Jaruzelska, K Borski, O Riess, et al.
Casopis Lekaru Ceskych
|
February 15, 1995
Molecular genetics of inherited diseases involving human chromosome 4
O Riess, H Schulz, T Träger, et al.
Brain Research. Molecular Brain Research
|
August 3, 2001
Functional characterization of the human Huntington's disease gene promoter
C Holzmann, T Schmidt, G Thiel, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
February 23, 2008
Microarray expression analysis reveals genetic pathways implicated in C621 synphilin-1-mediated toxicity
M Bonin, F P Marx, S Kautzmann, et al.
Genomics
|
December 1, 1991
Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene
B Weber, C Collins, D Kowbel, et al.
Human Genetics
|
February 1, 1997
Transmission distortion of the mutant alleles in spinocerebellar ataxia
O Riess, J T Epplen, G Amoiridis, et al.
Page
of 15