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	1.	Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene. [electronic resource] by Rosser, Lyndon G McKee, Shane Millar, David S Archer, Hayley Hughes, James Butler, Rachel Chuzhanova, Nadia Cooper, David N Lazarou, Lazarus P Producer: 20110714 In: Genomic medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Severe hypohidrotic ectodermal dysplasia in a girl caused by a de novo 9;X insertion that includes XIST and disrupts the EDA gene. [electronic resource] by Ørstavik, Karen Helene Knudsen, Gun Peggy S Nordgarden, Hilde Ormerod, Eli Strømme, Petter Lazarou, Lazarous P Rosser, Lyndon G Prescott, Trine Houge, Gunnar Producer: 20070928 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations. [electronic resource] by Liao, Chunyan Ashley, Neil Diot, Alan Morten, Karl Phadwal, Kanchan Williams, Andrew Fearnley, Ian Rosser, Lyndon Lowndes, Jo Fratter, Carl Ferguson, David J P Vay, Laura Quaghebeur, Gerardine Moroni, Isabella Bianchi, Stefania Lamperti, Costanza Downes, Susan M Sitarz, Kamil S Flannery, Padraig J Carver, Janet Dombi, Eszter East, Daniel Laura, Matilde Reilly, Mary M Mortiboys, Heather Prevo, Remko Campanella, Michelangelo Daniels, Matthew J Zeviani, Massimo Yu-Wai-Man, Patrick Simon, Anna Katharina Votruba, Marcela Poulton, Joanna Producer: 20170519 In: Neurology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)