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

Meredith Wilson

Department of Clinical Genetics

Western Sydney Genetics Program

Children's Hospital at Westmead

Sydney

Australia

[email]@chw.edu.au

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Clinical Genetics, Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, Australia. 2003 - 2008

References

  1. The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports. Wilson, M., Peters, G., Bennetts, B., McGillivray, G., Wu, Z.H., Poon, C., Algar, E. Am. J. Med. Genet. A (2008) [Pubmed]
  2. Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B. Wilson, M., Mowat, D., Dastot-Le Moal, F., Cacheux, V., Kääriäinen, H., Cass, D., Donnai, D., Clayton-Smith, J., Townshend, S., Curry, C., Gattas, M., Braddock, S., Kerr, B., Aftimos, S., Zehnwirth, H., Barrey, C., Goossens, M. Am. J. Med. Genet. A (2003) [Pubmed]
 
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