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

Ersan Kalay

Department of Human Genetics

Radboud University Nijmegen Medical Centre

P.O. Box 9101

6500 HB

Netherlands

[email]@*.umcn.nl

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Human Genetics, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB, Netherlands. 2005

References

  1. GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations. Kalay, E., Caylan, R., Kremer, H., de Brouwer, A.P., Karaguzel, A. Hear. Res. (2005) [Pubmed]
  2. Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. Kalay, E., Karaguzel, A., Caylan, R., Heister, A., Cremers, F.P., Cremers, C.W., Brunner, H.G., de Brouwer, A.P., Kremer, H. Hum. Mutat. (2005) [Pubmed]
 
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