Items where Author is "Millar, DS"

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Journal article

MILLAR, D.S., HORAN, M., CHUZHANOVA, N.A. and COOPER, D.N., 2010. Characterization of a functional intronic polymorphism in the human growth hormone (GH1) gene. Human Genomics, 4, pp. 289-301.

MILLAR, D.S., TYSOE, C., LAZAROU, L.P., PILZ, D.T., MOHAMMED, S., ANDERSON, K., CHUZHANOVA, N., COOPER, D.N. and BUTLER, R., 2010. An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene. Human Genomics, 4 (6), pp. 384-393.

WOLF, A., MILLAR, D.S., CALIEBE, A., HORAN, M., NEWSWAY, V., KUMPF, D., STEINMANN, K., CHEE, I.S., LEE, Y.H., MUTIRANGURA, A., PEPE, G., RICKARDS, O., SCHMIDTKE, J., SCHEMPP, W., CHUZHANOVA, N., KEHRER-SAWATZKI, H., KRAWCZAK, M. and COOPER, D.N., 2009. A gene conversion hotspot in the human growth hormone (GH1) gene promoter. Human Mutation, 30 (2), pp. 239-247.

SHAMSHER, M.K., CHUZHANOVA, N.A., FRIEDMAN, B., SCOPES, D.A., ALHAQ, A., MILLAR, D.S., COOPER, D.N. and BERG, L., 2000. Identification of an intronic regulatory element in the human protein C (PROC) gene. Human Genetics, 107, pp. 458-465.

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