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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Th Voit

Department of Pediatrics and Pediatric Neurology

University of Essen

Germany

[email]@uni-essen.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Pediatrics and Pediatric Neurology, University of Essen, Germany. 1998 - 2002

References

  1. Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD. Voit, T., Parano, E., Straub, V., Schröder, J.M., Schaper, J., Pavone, P., Falsaperla, R., Pavone, L., Herrmann, R. Neuromuscul. Disord. (2002) [Pubmed]
  2. Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus. Voit, T., Kutz, P., Leube, B., Neuen-Jacob, E., Schröder, J.M., Cavallotti, D., Vaccario, M.L., Schaper, J., Broich, P., Cohn, R., Baethmann, M., Göhlich-Ratmann, G., Scoppetta, C., Herrmann, R. Neuromuscul. Disord. (2001) [Pubmed]
  3. Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation. Voit, T., Cohn, R.D., Sperner, J., Leube, B., Sorokin, L., Toda, T., Herrmann, R. Neuromuscul. Disord. (1999) [Pubmed]
  4. Congenital muscular dystrophies: 1997 update. Voit, T. Brain Dev. (1998) [Pubmed]
 
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