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

J. Gecz

Department of Cytogenetics and Molecular Genetics

Women's and Children's Hospital


SA 5006



Name/email consistency: high



  • Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, Adelaide, SA 5006, Australia. 1997 - 2000


  1. Genes for cognitive function: developments on the X. Gécz, J., Mulley, J. Genome Res. (2000) [Pubmed]
  2. The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects. Gecz, J. Ann. Hum. Genet. (2000) [Pubmed]
  3. Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient. Gecz, J., Baker, E., Donnelly, A., Ming, J.E., McDonald-McGinn, D.M., Spinner, N.B., Zackai, E.H., Sutherland, G.R., Mulley, J.C. Hum. Genet. (1999) [Pubmed]
  4. Characterisation and expression of a large, 13.7 kb FMR2 isoform. Gecz, J., Mulley, J.C. Eur. J. Hum. Genet. (1999) [Pubmed]
  5. Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. Gécz, J., Barnett, S., Liu, J., Hollway, G., Donnelly, A., Eyre, H., Eshkevari, H.S., Baltazar, R., Grunn, A., Nagaraja, R., Gilliam, C., Peltonen, L., Sutherland, G.R., Baron, M., Mulley, J.C. Genomics (1999) [Pubmed]
  6. Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators. Gecz, J., Bielby, S., Sutherland, G.R., Mulley, J.C. Genomics (1997) [Pubmed]
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