Smith, B. N. Et Al. 2012. Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia. BRITISH JOURNAL OF HAEMATOLOGY , vol.158, no.1 , 146-149.

Smith, B. N., Evans, C., Ali, A., Ancliff, P. J., Hayee, B., Segal, A. W., ... Hall, G.(2012). Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia. BRITISH JOURNAL OF HAEMATOLOGY , vol.158, no.1, 146-149.

Smith, Bradley Et Al. "Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia," BRITISH JOURNAL OF HAEMATOLOGY , vol.158, no.1, 146-149, 2012

Smith, Bradley N. Et Al. "Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia." BRITISH JOURNAL OF HAEMATOLOGY , vol.158, no.1, pp.146-149, 2012

Smith, B. N. Et Al. (2012) . "Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia." BRITISH JOURNAL OF HAEMATOLOGY , vol.158, no.1, pp.146-149.

@article{article, author={Bradley N. Smith Et Al. }, title={Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia}, journal={BRITISH JOURNAL OF HAEMATOLOGY}, year=2012, pages={146-149} }