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Number of items: 10.

Jones, Robert H., Casbard, Angela, Carucci, Margherita, Cox, Catrin, Butler, Rachel, Alchami, Fouad, Madden, Tracie-Ann, Bale, Catherine, Bezecny, Pavel, Joffe, Johnathan, Moon, Sarah, Twelves, Chris, Venkitaraman, Ramachandran, Waters, Simon, Foxley, Andrew and Howell, Sacha J. 2020. Fulvestrant plus capivasertib versus placebo after relapse or progression on an aromatase inhibitor in metastatic, oestrogen receptor-positive breast cancer (FAKTION): a multicentre, randomised, controlled, phase 2 trial. Lancet Oncology 21 (3) , pp. 345-347. 10.1016/S1470-2045(19)30817-4

Davies, Rhian Siân, Smith, Christian, Edwards, Gwenllian, Butler, Rachel, Parry, Diane and Lester, Jason Francis 2017. Impact of cytological sampling on EGFR mutation testing in stage III-IV lung adenocarcinoma. Lung Cancer International 2017 , pp. 1-6. 10.1155/2017/9614938

Davies, R. S., Nelms, D. J., Butler, Rachel and Lester, J. F. 2016. Non-small cell lung cancer in South Wales: Are Exon 19 deletions and L858R different? Anticancer Research 36 (8) , pp. 4267-4271.

Richman, Susan D., Adams, Richard Alexander, Quirke, Phil, Butler, Rachel, Hemmings, Gemma, Chambers, Phil, Roberts, Helen, James, Michelle D., Wozniak, Sue, Bathia, Riya, Pugh, Cheryl, Maughan, Timothy Stanley and Jasani, Bharat 2015. Pre-trial inter-laboratory analytical validation of the FOCUS4 personalised therapy trial. Journal of Clinical Pathology 69 (1) , pp. 35-41. 10.1136/jclinpath-2015-203097

Millar, David Stuart, Tysoe, Carolyn, Lazarou, Lazarus P., Pilz, T., Mohammed, Shehla, Anderson, Katharine, Chuzhanova, Nadia, Cooper, David Neil and Butler, Rachel 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, Lyndon G., McKee, Shane, Millar, David Stuart, Archer, Hayley, Hughes, James, Butler, Rachel, Chuzhanova, Nadia, Cooper, David Neil and Lazarou, Lazarus P. 2008. Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene. Genomic Medicine 2 (3-4) , pp. 77-81. 10.1007/s11568-008-9026-9

Evans, Julie C., Archer, Hayley Louise, Colley, James, Ravn, Kirstine, Nielsen, Jytte Bieber, Kerr, Alison, Williams, Elizabeth, Christodoulou, John, Gécz, Jozef, Jardine, Philip E., Wright, Michael J., Pilz, Daniela, Lazarou, Lazarus, Cooper, David Neil, Sampson, Julian Roy, Butler, Rachel, Whatley, Sharon D. and Clarke, Angus John 2005. Early onset seizures and Rett-like features associated with mutations in CDKL5. European Journal of Human Genetics 13 (10) , pp. 1113-1120. 10.1038/sj.ejhg.5201451

Williams, David Wynne, Lewis, Michael Alexander Oxenham, Franzen, T., Lissett, V., Adams, C., Whittaker, David, Tysoe, C. and Butler, Rachel 2004. Sex determination by PCR analysis of DNA extracted from incinerated, deciduous teeth. Science & Justice 44 (2) , pp. 89-94. 10.1016/S1355-0306(04)71694-9

Emmerson, Paul, Maynard, Julie Helen, Jones, Sian, Butler, Rachel, Sampson, Julian Roy and Cheadle, Jeremy Peter 2003. Characterizing mutations in samples with low-level mosaicism by collection and analysis of DHPLC fractionated heteroduplexes. Human Mutation 21 (2) , pp. 112-115. 10.1002/humu.10159

Schwarz, Martin J., Malone, Geraldine M., Haworth, Andrea, Cheadle, Jeremy Peter, Meredith, Alison Linda, Gardner, Anne, Sawyer, I. Hilary, Connarty, Margaret, Dennis, Nick, Seller, Anneke, Harris, Ann, Taylor, Rohan, Dear, Simon, Middleton-Price, Helen, McMahon, Cathie, Mayall, Ed, McMahon, Rob, Barton, David E., Giles, Martin, Lindley, Victoria, Plaha, Davinder S., Price, Susan, Sharif, Abid, Cross, Gareth S., Dalton, Ann, Taylor, Graham, Wallace, Andrew, Tassabehji, Mayada, Whittaker, Joanne L., Butler, Rachel, Curtis, Ann, Pinkett, Ros, Gilfillan, Annette J., Brock, David J. H., Higgins, G. Scott, Lanyon, George, Miedzybrodzka, Zosia, Davidson, Mark, Graham, Colin A. and Hill, Alison J. M. 1995. Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories. Human Mutation 6 (4) , pp. 326-333. 10.1002/humu.1380060406

This list was generated on Tue Oct 26 04:14:18 2021 BST.