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Wim Wuyts

Department of Medical Genetics

University of Antwerp

Antwerp

Belgium

[email]@ua.ac.be

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, University of Antwerp, Antwerp, Belgium. 2005

References

  1. Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene. Wuyts, W., Reyniers, E., Ceuterick, C., Storm, K., de Barsy, T., Martin, J.J. Am. J. Med. Genet. A (2005) [Pubmed]
  2. Somatic and gonadal mosaicism in Hutchinson-Gilford progeria. Wuyts, W., Biervliet, M., Reyniers, E., D'Apice, M.R., Novelli, G., Storm, K. Am. J. Med. Genet. A (2005) [Pubmed]
  3. An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas. Wuyts, W., Radersma, R., Storm, K., Vits, L. Clin. Genet. (2005) [Pubmed]
 
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