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

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Jens Michael Hertz

Department of Clinical Genetics

Aarhus University Hospital

Aarhus C

Denmark

[email]@as.aaa.dk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Clinical Genetics, Aarhus University Hospital, Aarhus C, Denmark. 2005 - 2008

References

  1. MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome. Hertz, J.M., Juncker, I., Marcussen, N. Clin. Genet. (2008) [Pubmed]
  2. Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease. Hertz, J.M., Ostergaard, K., Juncker, I., Pedersen, S., Romstad, A., Møller, L.B., Güttler, F., Dupont, E. Eur. J. Neurol. (2006) [Pubmed]
  3. Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene. Hertz, J.M., Persson, U., Juncker, I., Segelmark, M. Hum. Genet. (2005) [Pubmed]
 
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