Meredith Wilson
Department of Clinical Genetics
Western Sydney Genetics Program
Children's Hospital at Westmead
Sydney
Australia
Name/email consistency: high
- 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)
- 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)