K. L. Friend

Common chromosomal fragile site FRA16D mutation in cancer cells (2005)

Finnis, M., Dayan, S., Hobson, L., Chenevix-Trench, G., Friend, K. L., Ried, Karin, ...

Neither the molecular basis for common fragile site DNA instability nor the contribution of this form of chromosomal instability to cancer is clearly understood. Fragile site FRA16D (16q23.2) is...

Common chromosomal fragile site FRA16D mutation in cancer cells (2005)

Finnis, M., Dayan, S., Hobson, L., Chenevix-Trench, G., Friend, K. L., Ried, Karin, ...

Neither the molecular basis for common fragile site DNA instability nor the contribution of this form of chromosomal instability to cancer is clearly understood. Fragile site FRA16D (16q23.2) is...

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus (2004)

Dudding, T. E., Friend, K. L., Schofield, P. R., Lee, S., Wilkinson, I., Richards, Robert Ian

Background: Most patients with pure nonprogressive congenital cerebellar ataxia have a sporadic form of unknown heredity and etiology. Several small families have been reported with a dominantly...

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...

Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus (2004)

Dudding, T. E., Friend, K. L., Schofield, P. R., Lee, S., Wilkinson, I., Richards, Robert Ian

Background: Most patients with pure nonprogressive congenital cerebellar ataxia have a sporadic form of unknown heredity and etiology. Several small families have been reported with a dominantly...

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM (1999)

Friend, K. L., Crimmins, D., Phan, T. G., Sue, C. M., Colley, A., Fung, Victor S. C., ...

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM (1999)

Friend, K. L., Crimmins, D., Phan, T. G., Sue, C. M., Colley, A., Fung, Victor S. C., ...

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM (1999)

Friend, K. L., Crimmins, D., Phan, T. G., Sue, C. M., Colley, A., Fung, Victor S. C., ...

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM (1999)

Friend, K. L., Crimmins, D., Phan, T. G., Sue, C. M., Colley, A., Fung, Victor S. C., ...