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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
August 6, 1999
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci
M Frontali, A Novelletto, G Annesi, et al.
Brain Research Bulletin
|
November 24, 2001
Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro
V Calabresi, S Guida, A Servadio, et al.
Human Biology
|
December 1, 1995
Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations
G Pepe, O Rickards, C Jodice, et al.
Cytogenetic and Genome Research
|
October 4, 2003
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders
E Mantuano, L Veneziano, C Jodice, et al.
Annals of Human Genetics
|
February 12, 1998
Population variation analysis at nine loci containing expressed trinucleotide repeats
C Jodice, B Giovannone, V Calabresi, et al.
Gene
|
July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1
E Mantuano, F Trettel, A S Olsen, et al.
Annals of Human Genetics
|
October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosome
F Persichetti, P Blasi, M Hammer, et al.
Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Genomics
|
September 15, 1996
Construction of a YAC contig covering human chromosome 6p22
P Malaspina, A Roetto, F Trettel, et al.
FEBS Letters
|
September 11, 2003
The AXH module: an independently folded domain common to ataxin-1 and HBP1
C de Chiara, C Giannini, S Adinolfi, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
August 6, 1999
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different loci
M Frontali, A Novelletto, G Annesi, et al.
Brain Research Bulletin
|
November 24, 2001
Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro
V Calabresi, S Guida, A Servadio, et al.
Human Biology
|
December 1, 1995
Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populations
G Pepe, O Rickards, C Jodice, et al.
Cytogenetic and Genome Research
|
October 4, 2003
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders
E Mantuano, L Veneziano, C Jodice, et al.
Annals of Human Genetics
|
February 12, 1998
Population variation analysis at nine loci containing expressed trinucleotide repeats
C Jodice, B Giovannone, V Calabresi, et al.
Gene
|
July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1
E Mantuano, F Trettel, A S Olsen, et al.
Annals of Human Genetics
|
October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosome
F Persichetti, P Blasi, M Hammer, et al.
Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Genomics
|
September 15, 1996
Construction of a YAC contig covering human chromosome 6p22
P Malaspina, A Roetto, F Trettel, et al.
FEBS Letters
|
September 11, 2003
The AXH module: an independently folded domain common to ataxin-1 and HBP1
C de Chiara, C Giannini, S Adinolfi, et al.
Page
of 3