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American Journal of Human Genetics
|
September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genes
K B Sims, L Ozelius, T Corey, et al.
Annals of Neurology
|
September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes
T Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
Neuron
|
January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletion
K B Sims, A de la Chapelle, R Norio, et al.
Molecular Biology & Medicine
|
December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia
X O Breakefield, L Ozelius, M A Bothwell, et al.
American Journal of Human Genetics
|
January 1, 1991
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred
D J Kwiatkowski, T G Nygaard, D E Schuback, et al.
Neuron
|
May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34
L Ozelius, P L Kramer, C B Moskowitz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 15, 2005
The North American Multiple System Atrophy Study Group
S Gilman, S J May, C W Shults, et al.
Neurology
|
October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutations
D Doheny, F Danisi, C Smith, et al.
Molecular Genetics and Metabolism
|
November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test
R Saunders-Pullman, N Blau, K Hyland, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
American Journal of Human Genetics
|
September 1, 1989
Norrie disease gene is distinct from the monoamine oxidase genes
K B Sims, L Ozelius, T Corey, et al.
Annals of Neurology
|
September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes
T Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
Neuron
|
January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletion
K B Sims, A de la Chapelle, R Norio, et al.
Molecular Biology & Medicine
|
December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia
X O Breakefield, L Ozelius, M A Bothwell, et al.
American Journal of Human Genetics
|
January 1, 1991
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred
D J Kwiatkowski, T G Nygaard, D E Schuback, et al.
Neuron
|
May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34
L Ozelius, P L Kramer, C B Moskowitz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 15, 2005
The North American Multiple System Atrophy Study Group
S Gilman, S J May, C W Shults, et al.
Neurology
|
October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutations
D Doheny, F Danisi, C Smith, et al.
Molecular Genetics and Metabolism
|
November 16, 2004
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test
R Saunders-Pullman, N Blau, K Hyland, et al.
Page
of 4