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

M. Tassabehji

Department of Medical Genetics

St Mary's Hospital




Name/email consistency: high



  • Department of Medical Genetics, St Mary's Hospital, Manchester, UK. 1997 - 2003
  • University Department of Medical Genetics and Regional Genetics Service, St Mary's Hospital, Manchester M13 0JH, UK. 1998


  1. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations. Tassabehji, M. Hum. Mol. Genet. (2003) [Pubmed]
  2. A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome. Tassabehji, M., Carette, M., Wilmot, C., Donnai, D., Read, A.P., Metcalfe, K. Eur. J. Hum. Genet. (1999) [Pubmed]
  3. An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa. Tassabehji, M., Metcalfe, K., Hurst, J., Ashcroft, G.S., Kielty, C., Wilmot, C., Donnai, D., Read, A.P., Jones, C.J. Hum. Mol. Genet. (1998) [Pubmed]
  4. Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis. Tassabehji, M., Metcalfe, K., Donnai, D., Hurst, J., Reardon, W., Burch, M., Read, A.P. Hum. Mol. Genet. (1997) [Pubmed]
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