Found: 13
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Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
- Published in:
- 2008
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- Publication type:
- Journal Article
Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?
- Published in:
- Neurogenetics, 2008, v. 9, n. 2, p. 143, doi. 10.1007/s10048-008-0123-7
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- Publication type:
- Article
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis.
- Published in:
- Genetic Epidemiology, 1987, v. 4, n. 5, p. 377, doi. 10.1002/gepi.1370040506
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- Publication type:
- Article
Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.
- Published in:
- Nature, 1988, v. 332, n. 6161, p. 268, doi. 10.1038/332268a0
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- Publication type:
- Article
The North American Multiple System Atrophy Study Group.
- Published in:
- Journal of Neural Transmission, 2005, v. 112, n. 12, p. 1687, doi. 10.1007/s00702-005-0381-6
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- Publication type:
- Article
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 88, doi. 10.1111/j.1399-0004.1994.tb04000.x
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- Publication type:
- Article
Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.
- Published in:
- 2001
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- Publication type:
- journal article
Association studies of Parkinson's disease and parkin polymorphisms.
- Published in:
- 2000
- By:
- Publication type:
- letter
Genetic linkage studies in autosomal dominant parkinsonism: Evaluation of seven candidate genes.
- Published in:
- Annals of Neurology, 1994, v. 36, n. 3, p. 387, doi. 10.1002/ana.410360310
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- Publication type:
- Article
Haplotype analysis at the DYT1 Locus in ashkenazi jewish patients with occupational hand dystonia.
- Published in:
- Movement Disorders, 1996, v. 11, n. 2, p. 163, doi. 10.1002/mds.870110208
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- Publication type:
- Article
Principles of molecular genetics/Dystonia.
- Published in:
- Movement Disorders, 1992, v. 7, n. S1, p. 2, doi. 10.1002/mds.870070503
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- Publication type:
- Article
Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32–34.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 2, p. 141
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- Publication type:
- Article
Cortical sensorimotor alterations classify clinical phenotype and putative genotype of spasmodic dysphonia.
- Published in:
- European Journal of Neurology, 2016, v. 23, n. 10, p. 1517, doi. 10.1111/ene.13067
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- Publication type:
- Article