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Genetic linkage
Citations 41-50 of 81 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese
- Y. Onodera, M. Aoki, H. Mizuno, H. Warita, Y. Shiga, and Y. Itoyama
Neurology 2006; 67: 1300-1302.
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- ARTICLES
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27
- B. A. Neubauer, I. Stefanova, C. A. Hübner, E. Neumaier-Probst, J. Bohl, H. C. Oppermann, H. Stöß, A. Hahn, U. Stephani, A. Kohlschütter, and A. Gal
Neurology 2006; 67: 587-591.
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- BRIEF COMMUNICATIONS
Charcot–Marie–Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene
- D. Kabzinska, H. Drac, D. L. Sherman, A. Kostera-Pruszczyk, P. J. Brophy, A. Kochanski, and I. Hausmanowa-Petrusewicz
Neurology 2006; 66: 745-747.
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- BRIEF COMMUNICATIONS
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
- M. F. Waters, D. Fee, K. P. Figueroa, D. Nolte, U. Müller, J. Advincula, H. Coon, V. G. Evidente, and S. M. Pulst
Neurology 2005; 65: 1111-1113.
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- BRIEF COMMUNICATIONS
Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci
- A. Kochanski, M. Kennerson, M. Kawulak, B. Ryniewicz, K. Rowinska-Marcinska, G. Walizada, A. Nowakowski, I. Hausmanowa-Petrusewicz, and G. A. Nicholson
Neurology 2005; 64: 533-535.
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- ARTICLES
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
- T. E. Dudding, K. Friend, P. W. Schofield, S. Lee, I. A. Wilkinson, and R. I. Richards
Neurology 2004; 63: 2288-2292.
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Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy
- J. C. Jen, H. Wang, H. Lee, C. Sabatti, R. Trent, I. Hannigan, K. Brantberg, G. M. Halmagyi, S. F. Nelson, and R. W. Baloh
Neurology 2004; 63: 2376-2379.
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- EDITORIALS
Turning on the heat: The search for febrile seizure genes
- Melodie Winawer and Dale Hesdorffer
Neurology 2004; 63: 1770-1771.
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- ARTICLES
Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18
- J. Nakayama, N. Yamamoto, K. Hamano, N. Iwasaki, M. Ohta, S. Nakahara, A. Matsui, E. Noguchi, and T. Arinami
Neurology 2004; 63: 1803-1807.
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- BRIEF COMMUNICATIONS
A novel candidate region for ALS on chromosome 14q11.2
- M. J. Greenway, M. D. Alexander, S. Ennis, B. J. Traynor, B. Corr, E. Frost, A. Green, and O. Hardiman
Neurology 2004; 63: 1936-1938.
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