Adelaide Research & Scholarship
Browsing "Paediatrics publications" by Author Laing, N.
Showing results 1 to 4 of 4
Preview | Issue Date | Title | Author(s) |
| 1995 | A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy | Laing, N.; Wilton, S.; Akkari, P.; Dorosz, S.; Boundy, K.; Kneebone, C.; Blumbergs, P.; White, S.; Watkins, H.; Love, D.; Haan, E. |
| 1995 | Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation | Hunt, C.; Eyre, H.; Akkari, P.; Meredith, C.; Dorosz, S.; Wilton, S.; Callen, D.; Laing, N.; Baker, E. |
| 1995 | Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization | Eyre, H.; Akkari, P.; Wilton, S.; Callen, D.; Baker, E.; Laing, N. |
| 2001 | Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome | Kelberman, D.; Tyson, J.; Chandler, D.; McInerney, A.; Slee, J.; Albert, D.; Aymat, A.; Botma, M.; Calvert, M.; Goldblatt, J.; Haan, E.; Laing, N.; Lim, J.; Malcolm, S.; Singer, S.; Winter, R.; Bitner-Glindzicz, M. |