Items where Author is "Lazarou, LP"

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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.

ROSSER, L.G., MCKEE, S., MILLER, D.S., ARCHER, H., HUGHES, J., BUTLER, R., CHUZHANOVA, N., COOPER, D.N. and LAZAROU, L.P., 2008. Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 genenon-identical paternally-derived microdeletions in the MECP2 gene. Genomic Medicine, 2, pp. 77-81.

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