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	1.	Subcortical white matter abnormalities because of previously undescribed de-novo 14q12-q13.1 triplication. [electronic resource] by Rea, Gillian Stallings, Ray L Mullarkey, Marice McKinstry, C Steven McManus, David Morrison, Patrick J Producer: 20130911 In: Clinical dysmorphology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3). [electronic resource] by Gallagher, Louise Becker, Kristin Kearney, Geraldine Dunlop, Adam Stallings, Ray Green, Andrew Fitzgerald, Michael Gill, Michael Producer: 20030804 In: Journal of autism and developmental disorders vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Orchestrating osteogenic differentiation of mesenchymal stem cells--identification of placental growth factor as a mechanosensitive gene with a pro-osteogenic role. [electronic resource] by McCoy, Ryan J Widaa, Amro Watters, Karen M Wuerstle, Maximilian Stallings, Ray L Duffy, Garry P O'Brien, Fergal J Producer: 20140917 In: Stem cells (Dayton, Ohio) vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome? [electronic resource] by Cunningham, Joan Sales, Mark Pearce, Andrew Howard, Julie Stallings, Ray Telford, Nicholas Wilkie, Rosalie Huntly, Brian Thomas, Angela O'Marcaigh, Aengus Will, Andrew Pratt, Norman Producer: 20030123 In: British journal of haematology vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Minimal residual disease detection in childhood acute lymphoblastic leukaemia patients at multiple time-points reveals high levels of concordance between molecular and immunophenotypic approaches. [electronic resource] by Ryan, Jacqueline Quinn, Fiona Meunier, Armelle Boublikova, Ludmila Crampe, Mireille Tewari, Prerna O'Marcaigh, Aengus Stallings, Ray Neat, Michael O'Meara, Ann Breatnach, Fin McCann, Shaun Browne, Paul Smith, Owen Lawler, Mark Producer: 20090220 In: British journal of haematology vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Methyl-CpG-binding domain sequencing reveals a prognostic methylation signature in neuroblastoma. [electronic resource] by Decock, Anneleen Ongenaert, Maté Cannoodt, Robrecht Verniers, Kimberly De Wilde, Bram Laureys, Geneviève Van Roy, Nadine Berbegall, Ana P Bienertova-Vasku, Julie Bown, Nick Clément, Nathalie Combaret, Valérie Haber, Michelle Hoyoux, Claire Murray, Jayne Noguera, Rosa Pierron, Gaelle Schleiermacher, Gudrun Schulte, Johannes H Stallings, Ray L Tweddle, Deborah A De Preter, Katleen Speleman, Frank Vandesompele, Jo Producer: 20161213 In: Oncotarget vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A multilocus technique for risk evaluation of patients with neuroblastoma. [electronic resource] by Ambros, Inge M Brunner, Bettina Aigner, Gerhard Bedwell, Clare Beiske, Klaus Bénard, Jean Bown, Nick Combaret, Valerie Couturier, Jerome Defferrari, Raffaella Gross, Nicole Jeison, Marta Lunec, John Marques, Barbara Martinsson, Tommy Mazzocco, Katia Noguera, Rosa Schleiermacher, Gudrun Speleman, Frank Stallings, Ray Tonini, Gian Paolo Tweddle, Deborah A Valent, Alexander Vicha, Ales Roy, Nadine Van Villamon, Eva Ziegler, Andrea Preuner, Sandra Drobics, Mario Ladenstein, Ruth Amann, Gabriele Schuit, Robert J L Pötschger, Ulrike Ambros, Peter F Producer: 20110815 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. [electronic resource] by Heinzen, Erin L Radtke, Rodney A Urban, Thomas J Cavalleri, Gianpiero L Depondt, Chantal Need, Anna C Walley, Nicole M Nicoletti, Paola Ge, Dongliang Catarino, Claudia B Duncan, John S Kasperaviciūte, Dalia Tate, Sarah K Caboclo, Luis O Sander, Josemir W Clayton, Lisa Linney, Kristen N Shianna, Kevin V Gumbs, Curtis E Smith, Jason Cronin, Kenneth D Maia, Jessica M Doherty, Colin P Pandolfo, Massimo Leppert, David Middleton, Lefkos T Gibson, Rachel A Johnson, Michael R Matthews, Paul M Hosford, David Kälviäinen, Reetta Eriksson, Kai Kantanen, Anne-Mari Dorn, Thomas Hansen, Jörg Krämer, Günter Steinhoff, Bernhard J Wieser, Heinz-Gregor Zumsteg, Dominik Ortega, Marcos Wood, Nicholas W Huxley-Jones, Julie Mikati, Mohamad Gallentine, William B Husain, Aatif M Buckley, Patrick G Stallings, Ray L Podgoreanu, Mihai V Delanty, Norman Sisodiya, Sanjay M Goldstein, David B Producer: 20100621 In: American journal of human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)