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Showing results (11-20 of 24) with videos related to

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Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Gene|December 23, 1999
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosomeF Trettel, E Mantuano, V Calabresi, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Brain : a Journal of Neurology|May 1, 1997
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13L Calandriello, L Veneziano, A Francia, et al.
Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.
Journal of Molecular Evolution|June 1, 1997
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homologyP Malaspina, B M Ciminelli, L Viggiano, et al.
Human Biology|October 26, 2000
Latitude-correlated genetic polymorphisms: selection or gene flow?B M Ciminelli, C Jodice, R Scozzari, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Gene|December 23, 1999
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosomeF Trettel, E Mantuano, V Calabresi, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Brain : a Journal of Neurology|May 1, 1997
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13L Calandriello, L Veneziano, A Francia, et al.
Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.
Journal of Molecular Evolution|June 1, 1997
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homologyP Malaspina, B M Ciminelli, L Viggiano, et al.
Human Biology|October 26, 2000
Latitude-correlated genetic polymorphisms: selection or gene flow?B M Ciminelli, C Jodice, R Scozzari, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Pageof 3