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Genetic linkage
Citations 51-60 of 81 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations
- Y. Hatano, K. Sato, B. Elibol, H. Yoshino, Y. Yamamura, V. Bonifati, H. Shinotoh, M. Asahina, S. Kobayashi, A. R. Ng, R. L. Rosales, S. Hassin-Baer, Y. Shinar, C. S. Lu, H. C. Chang, Y. H. Wu-Chou, F. B. Ataç, T. Kobayashi, T. Toda, Y. Mizuno, and N. Hattori
Neurology 2004; 63: 1482-1485.
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- BRIEF COMMUNICATIONS
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly
- U. Aguglia, A. Gambardella, G. J. Breedveld, R. L. Oliveri, E. Le Piane, D. Messina, A. Quattrone, and P. Heutink
Neurology 2004; 62: 1613-1615.
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- ARTICLES
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family
- B. P.C. van de Warrenburg, D. S. Verbeek, S. J. Piersma, F. A.M. Hennekam, P. L. Pearson, N. V.A.M. Knoers, H. P.H. Kremer, and R. J. Sinke
Neurology 2003; 61: 1760-1765.
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- BRIEF COMMUNICATIONS
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2
- L. Palenzuela, A.L. Andreu, J. Gàmez, M.R. Vilà, T. Kunimatsu, A. Meseguer, C. Cervera, I. Fernandez Cadenas, P.F.M. van der Ven, T.G. Nygaard, E. Bonilla, and M. Hirano
Neurology 2003; 61: 404-406.
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- BRIEF COMMUNICATIONS
A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia
- P.A. Wilkinson, A.H. Crosby, C. Turner, H. Patel, N.W. Wood, A.H. Schapira, and T.T. Warner
Neurology 2003; 61: 235-238.
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- ARTICLES
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21
- A. Rajab, G. H. Mochida, A. Hill, V. Ganesh, A. Bodell, A. Riaz, P. E. Grant, Y. Y. Shugart, and C. A. Walsh
Neurology 2003; 60: 1664-1667.
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- BRIEF COMMUNICATIONS
High rate of constitutional chromosomal rearrangements in apparently sporadic ALS
- T. Meyer, B. Alber, K. Roemer, T. Martin, V.M. Kalscheuer, E. Göttert, K.D. Zang, A.C. Ludolph, H.-H. Ropers, and J. Prudlo
Neurology 2003; 60: 1348-1350.
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- BRIEF COMMUNICATIONS
Benign adult familial myoclonic epilepsy: Genetic heterogeneity and allelism with ADCME
- F.A. de Falco, P. Striano, A. de Falco, S. Striano, R. Santangelo, A. Perretti, P. Balbi, M. Cecconi, and F. Zara
Neurology 2003; 60: 1381-1385.
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- ARTICLES
The gene for HMSN2C maps to 12q23-24: A region of neuromuscular disorders
- C. J. Klein, J. M. Cunningham, E. J. Atkinson, D. J. Schaid, S. J. Hebbring, S. A. Anderson, D. M. Klein, P. J.B. Dyck, W. J. Litchy, S. N. Thibodeau, and P. J. Dyck
Neurology 2003; 60: 1151-1156.
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- ARTICLES
A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14
- C. A. Hodgkinson, S. Bohlega, S. N. Abu–Amero, E. Cupler, M. Kambouris, B. F. Meyer, and V. A. Bharucha
Neurology 2002; 59: 1905-1909.
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