David S. Millar
Institute of Medical Genetics
Cardiff University
Heath Park
UK
Name/email consistency: high
- Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) gene. Millar, D.S., Horan, M., Chuzhanova, N.A., Cooper, D.N. Hum. Genomics (2010)
- Growth hormone (GH1) gene variation and the growth hormone receptor (GHR) exon 3 deletion polymorphism in a West-African population. Millar, D.S., Lewis, M.D., Horan, M., Newsway, V., Rees, D.A., Easter, T.E., Pepe, G., Rickards, O., Norin, M., Scanlon, M.F., Krawczak, M., Cooper, D.N. Mol. Cell. Endocrinol. (2008)
- Molecular analysis of the genotype-phenotype relationship in factor X deficiency. Millar, D.S., Elliston, L., Deex, P., Krawczak, M., Wacey, A.I., Reynaud, J., Nieuwenhuis, H.K., Bolton-Maggs, P., Mannucci, P.M., Reverter, J.C., Cachia, P., Pasi, K.J., Layton, D.M., Cooper, D.N. Hum. Genet. (2000)
- Molecular genetic analysis of severe protein C deficiency. Millar, D.S., Johansen, B., Berntorp, E., Minford, A., Bolton-Maggs, P., Wensley, R., Kakkar, V., Schulman, S., Torres, A., Bosch, N., Cooper, D.N. Hum. Genet. (2000)
- Molecular analysis of the genotype-phenotype relationship in factor VII deficiency. Millar, D.S., Kemball-Cook, G., McVey, J.H., Tuddenham, E.G., Mumford, A.D., Attock, G.B., Reverter, J.C., Lanir, N., Parapia, L.A., Reynaud, J., Meili, E., von Felton, A., Martinowitz, U., Prangnell, D.R., Krawczak, M., Cooper, D.N. Hum. Genet. (2000)
