Items where Author is "Millar, DS"

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Number of items: 4.

Journal article

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. ISSN 1473-9542

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.

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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