Investigation of muscle disease.

Por Mastaglia, F L, Laing, N G
Publicado em 1996

Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

Por North, K N, Laing, N G, Wallgren-Pettersson, C
Publicado em 1997

A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.

Por Walker, A P, Laing, N G, Yamada, T, Chandler, D C, Kakulas, B A, Bartlett, R J
Publicado em 1992

Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.

Por Laing, N G, Akkari, P A, Chandler, D C, Thomas, H E, Layton, M G, Mears, M E, Kakulas, B A
Publicado em 1990

RFLP for Duchenne muscular dystrophy cDNA clone 30-2.

Por Walker, A P, Bartlett, R J, Laing, N G, Siddique, T, Yamaoka, L H, Chen, J C, Hung, W Y, Roses, A D
Publicado em 1988

RFLP for Duchenne muscular dystrophy cDNA clone 44-1.

Por Laing, N G, Siddique, T, Bartlett, R J, Yamaoka, L H, Chen, J C, Walker, A P, Hung, W Y, Roses, A D
Publicado em 1988

Autosomal dominant distal myopathy: linkage to chromosome 14.

Por Laing, N G, Laing, B A, Meredith, C, Wilton, S D, Robbins, P, Honeyman, K, Dorosz, S, Kozman, H, Mastaglia, F L, Kakulas, B A
Publicado em 1995

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy

Por Lamont, P J, Udd, B, Mastaglia, F L, de Visser, M, Hedera, P, Voit, T, Bridges, L R, Fabian, V, Rozemuller, A, Laing, N G
Publicado em 2006

Assignment of a gene (NEM1) for autosomal dominant nemaline myopathy to chromosome 1

Por Laing, N. G., Majda, B. T., Akkari, P. A., Layton, M. G., Mulley, J. C., Phillips, H., Haan, E. A., White, S. J., Beggs, A. H., Kunkel, L. M., Groth, D. M., Boundy, K. L., Kneebone, C. S., Blumberg, P. C., Wilton, S. D., Speer, M. C., Kakulas, B. A.
Publicado em 1992