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	1.	Variant detection sensitivity and biases in whole genome and exome sequencing. [electronic resource] by Meynert, Alison M Ansari, Morad FitzPatrick, David R Taylor, Martin S Producer: 20141012 In: BMC bioinformatics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Quantifying single nucleotide variant detection sensitivity in exome sequencing. [electronic resource] by Meynert, Alison M Bicknell, Louise S Hurles, Matthew E Jackson, Andrew P Taylor, Martin S Producer: 20140206 In: BMC bioinformatics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. [electronic resource] by Handley, Mark T Mégarbané, André Meynert, Alison M Brown, Stephen Freyer, Elisabeth Taylor, Martin S Jackson, Ian J Aligianis, Irene A Producer: 20140731 In: Molecular genetics & genomic medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical and molecular characterization of ovarian carcinoma displaying isolated lymph node relapse. [electronic resource] by Hollis, Robert L Carmichael, Juliet Meynert, Alison M Churchman, Michael Hallas-Potts, Amelia Rye, Tzyvia MacKean, Melanie Nussey, Fiona Semple, Colin A Herrington, C Simon Gourley, Charlie Producer: 20200224 In: American journal of obstetrics and gynecology vol. 221 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations. [electronic resource] by Hollis, Robert L Meynert, Alison M Churchman, Michael Rye, Tzyvia Mackean, Melanie Nussey, Fiona Arends, Mark J Sims, Andrew H Semple, Colin A Herrington, C Simon Gourley, Charlie Producer: 20180814 In: BMC cancer vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. [electronic resource] by Taylor, Rachel L Handley, Mark T Waller, Sarah Campbell, Christopher Urquhart, Jill Meynert, Alison M Ellingford, Jamie M Donnelly, Deirdre Wilcox, Gisela Lloyd, I Chris Mundy, Helen FitzPatrick, David R Deshpande, Charu Clayton-Smith, Jill Black, Graeme C Producer: 20170623 In: Investigative ophthalmology & visual science vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. [electronic resource] by Kerr, Shona M Klaric, Lucija Halachev, Mihail Hayward, Caroline Boutin, Thibaud S Meynert, Alison M Semple, Colin A Tuiskula, Annukka M Swan, Heikki Santoyo-Lopez, Javier Vitart, Veronique Haley, Chris Dean, John Miedzybrodzka, Zosia Aitman, Timothy J Wilson, James F Producer: 20201027 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	CAG-encoded polyglutamine length polymorphism in the human genome. [electronic resource] by Butland, Stefanie L Devon, Rebecca S Huang, Yong Mead, Carri-Lyn Meynert, Alison M Neal, Scott J Lee, Soo Sen Wilkinson, Anna Yang, George S Yuen, Macaire M S Hayden, Michael R Holt, Robert A Leavitt, Blair R Ouellette, B F Francis Producer: 20070711 In: BMC genomics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. [electronic resource] by Ansari, Morad Poke, Gemma Ferry, Quentin Williamson, Kathleen Aldridge, Roland Meynert, Alison M Bengani, Hemant Chan, Cheng Yee Kayserili, Hülya Avci, Sahin Hennekam, Raoul C M Lampe, Anne K Redeker, Egbert Homfray, Tessa Ross, Alison Falkenberg Smeland, Marie Mansour, Sahar Parker, Michael J Cook, Jacqueline A Splitt, Miranda Fisher, Richard B Fryer, Alan Magee, Alex C Wilkie, Andrew Barnicoat, Angela Brady, Angela F Cooper, Nicola S Mercer, Catherine Deshpande, Charu Bennett, Christopher P Pilz, Daniela T Ruddy, Deborah Cilliers, Deirdre Johnson, Diana S Josifova, Dragana Rosser, Elisabeth Thompson, Elizabeth M Wakeling, Emma Kinning, Esther Stewart, Fiona Flinter, Frances Girisha, Katta M Cox, Helen Firth, Helen V Kingston, Helen Wee, Jamie S Hurst, Jane A Clayton-Smith, Jill Tolmie, John Vogt, Julie Tatton-Brown, Katrina Chandler, Kate Prescott, Katrina Wilson, Louise Behnam, Mahdiyeh McEntagart, Meriel Davidson, Rosemarie Lynch, Sally-Ann Sisodiya, Sanjay Mehta, Sarju G McKee, Shane A Mohammed, Shehla Holden, Simon Park, Soo-Mi Holder, Susan E Harrison, Victoria McConnell, Vivienne Lam, Wayne K Green, Andrew J Donnai, Dian Bitner-Glindzicz, Maria Donnelly, Deirdre E Nellåker, Christoffer Taylor, Martin S FitzPatrick, David R Producer: 20150518 In: Journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)