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American Journal of Human Genetics
|
September 1, 1996
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia
A Filla, G De Michele, F Cavalcanti, et al.
Acta Neurologica
|
August 1, 1992
Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in Italy
L Di Maio, S Boiano, F Squitieri, et al.
Human Molecular Genetics
|
November 13, 1998
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia
G De Michele, F Cavalcanti, C Criscuolo, et al.
Arquivos De Neuro-Psiquiatria
|
May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxia
I V Schwartz, L B Jardim, A C Puga, et al.
Neural Networks : the Official Journal of the International Neural Network Society
|
February 8, 2008
Interactive data analysis and clustering of genomic data
A Ciaramella, S Cocozza, F Iorio, et al.
Journal of Neurology
|
April 29, 1998
Determinants of onset age in Friedreich's ataxia
G De Michele, A Filla, C Criscuolo, et al.
Neuropediatrics
|
February 1, 1996
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 cases
G De Michele, L Di Maio, A Filla, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family
R Rizzi, V Carelli, L Monari, et al.
Journal of Medical Genetics
|
April 3, 2004
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype
M Giacchetti, A Monticelli, I De Biase, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
September 30, 1987
[Strategy for the identification of new DNA polymorphisms: diagnostic application as genetic markers]
S Cocozza, A Monticelli, S Garofalo, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 81) with videos related to
Sort By:
Page
of 9
American Journal of Human Genetics
|
September 1, 1996
The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia
A Filla, G De Michele, F Cavalcanti, et al.
Acta Neurologica
|
August 1, 1992
Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in Italy
L Di Maio, S Boiano, F Squitieri, et al.
Human Molecular Genetics
|
November 13, 1998
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia
G De Michele, F Cavalcanti, C Criscuolo, et al.
Arquivos De Neuro-Psiquiatria
|
May 29, 1999
Clinical and molecular studies in five Brazilian cases of Friedreich ataxia
I V Schwartz, L B Jardim, A C Puga, et al.
Neural Networks : the Official Journal of the International Neural Network Society
|
February 8, 2008
Interactive data analysis and clustering of genomic data
A Ciaramella, S Cocozza, F Iorio, et al.
Journal of Neurology
|
April 29, 1998
Determinants of onset age in Friedreich's ataxia
G De Michele, A Filla, C Criscuolo, et al.
Neuropediatrics
|
February 1, 1996
Childhood onset of Friedreich ataxia: a clinical and genetic study of 36 cases
G De Michele, L Di Maio, A Filla, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family
R Rizzi, V Carelli, L Monari, et al.
Journal of Medical Genetics
|
April 3, 2004
Mitochondrial DNA haplogroups influence the Friedreich's ataxia phenotype
M Giacchetti, A Monticelli, I De Biase, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
September 30, 1987
[Strategy for the identification of new DNA polymorphisms: diagnostic application as genetic markers]
S Cocozza, A Monticelli, S Garofalo, et al.
Page
of 9