Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy
Ionasescu, V V, Searby, C, Ionasescu, R, Neuhaus, I M, Werner, R
Published in Neurology (01.08.1996)
Published in Neurology (01.08.1996)
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Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma
Ohlendieck, K, Matsumura, K, Ionasescu, V V, Towbin, J A, Bosch, E P, Weinstein, S L, Sernett, S W, Campbell, K P
Published in Neurology (01.04.1993)
Published in Neurology (01.04.1993)
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Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene
Ionasescu, Victor V., Searby, Charles C., Ionasescu, Rebecca, Reisin, Ricardo, Ruggieri, Victor, Arberas, Claudia
Published in Muscle & nerve (01.10.1997)
Published in Muscle & nerve (01.10.1997)
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Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy
IONASESCU, V. V, TROFATTER, J, HAINES, J. L, SUMMERS, A. M, IONASESCU, R, SEARBY, C
Published in American journal of human genetics (01.06.1991)
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Published in American journal of human genetics (01.06.1991)
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X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic study
Ionasescu, V V, Trofatter, J, Haines, J L, Summers, A M, Ionasescu, R, Searby, C
Published in Muscle & nerve (01.03.1992)
Published in Muscle & nerve (01.03.1992)
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Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplication
Ionasescu, V V, Ionasescu, R, Searby, C, Barker, D F
Published in Human molecular genetics (01.04.1993)
Published in Human molecular genetics (01.04.1993)
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Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy
Ionasescu, V V, Trofatter, J, Haines, J L, Ionasescu, R, Searby, C
Published in Neurology (01.04.1992)
Published in Neurology (01.04.1992)
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New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy
Ionasescu, V., Searby, Ch, Ionasescu, R., Meschino, W.
Published in Neuromuscular disorders : NMD (01.07.1995)
Published in Neuromuscular disorders : NMD (01.07.1995)
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A Dejerine-Sottas neuropathy family with a gene mapped on chromosome 8
Ionasescu, Victor V., Kimura, Jun, Searby, Charles C., Smith Jr, Wilbur L., Ross, Mark A., Ionasescu, Rebecca
Published in Muscle & nerve (01.03.1996)
Published in Muscle & nerve (01.03.1996)
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Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35
MATHEWS, K. D, MILLS, K. A, BOSCH, E. P, IONASESCU, V. V, WILES, K. R, BUETOW, K. H, MURRAY, J. C
Published in American journal of human genetics (01.08.1992)
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Published in American journal of human genetics (01.08.1992)
Journal Article
Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V
Antonellis, Anthony, Ellsworth, Rachel E., Sambuughin, Nyamkhishig, Puls, Imke, Abel, Annette, Lee-Lin, Shih-Queen, Jordanova, Albena, Kremensky, Ivo, Christodoulou, Kyproula, Middleton, Lefkos T., Sivakumar, Kumaraswamy, Ionasescu, Victor, Funalot, Benoit, Vance, Jeffery M., Goldfarb, Lev G., Fischbeck, Kenneth H., Green, Eric D.
Published in American journal of human genetics (01.05.2003)
Published in American journal of human genetics (01.05.2003)
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Linkage studies of X-linked recessive spastic paraplegia using DNA probes
Kenwrick, S, Ionasescu, V, Ionasescu, G, Searby, C, King, A, Dubowitz, M, Davies, K E
Published in Human genetics (01.07.1986)
Published in Human genetics (01.07.1986)
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