M. Tassabehji
Department of Medical Genetics
St Mary's Hospital
Manchester
UK
Name/email consistency: high
- Williams-Beuren syndrome: a challenge for genotype-phenotype correlations. Tassabehji, M. Hum. Mol. Genet. (2003)
- 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)
- 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)
- 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)
