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

K.H. Orstavik

Department of Medical Genetics

Ullevål Hospital

Norway

[email]@ioks.uio.no

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, Ullevål Hospital, Norway. 1998 - 2000

References

  1. Absence of correlation between X chromosome inactivation pattern and plasma concentration of factor VIII and factor IX in carriers of haemophilia A and B. Orstavik, K.H., Scheibel, E., Ingerslev, J., Schwartz, M. Thromb. Haemost. (2000) [Pubmed]
  2. Severe craniofacial malformations and deglutition dysfunction in a brother and sister: new syndrome?. Orstavik, K.H., Tangsrud, S.E., Nordshus, T., Lange, J.E., Renolen, O., Lyberg, T. Am. J. Med. Genet. (1998) [Pubmed]
  3. X chromosome inactivation in carriers of Barth syndrome. Orstavik, K.H., Orstavik, R.E., Naumova, A.K., D'Adamo, P., Gedeon, A., Bolhuis, P.A., Barth, P.G., Toniolo, D. Am. J. Hum. Genet. (1998) [Pubmed]
 
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