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	1.	Using familial information for variant filtering in high-throughput sequencing studies. [electronic resource] by Bahlo, Melanie Tankard, Rick Lukic, Vesna Oliver, Karen L Smith, Katherine R Producer: 20141203 In: Human genetics vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery. [electronic resource] by Oliver, Karen L Lukic, Vesna Freytag, Saskia Scheffer, Ingrid E Berkovic, Samuel F Bahlo, Melanie Producer: 20160412 In: Neurology. Genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genes. [electronic resource] by Oliver, Karen L Lukic, Vesna Thorne, Natalie P Berkovic, Samuel F Scheffer, Ingrid E Bahlo, Melanie Producer: 20151201 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Genetic Analysis of Patients Who Experienced Awareness with Recall while under General Anesthesia. [electronic resource] by Sleigh, Jamie W Leslie, Kate Davidson, Andrew J Amor, David J Diakumis, Peter Lukic, Vesna Lockhart, Paul J Bahlo, Melanie Producer: 20200330 In: Anesthesiology vol. 131 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	None [electronic resource] by Stamenkovic, Miroslav Lukic, Vesna Suvakov, Sonja Simic, Tatjana Sencanic, Ivan Pljesa-Ercegovac, Marija Jaksic, Vesna Babovic, Sinisa Matic, Marija Radosavljevic, Aleksandra Savic-Radojevic, Ana Djukic, Tatjana Publication details: International journal of ophthalmology 2018 In: International journal of ophthalmology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss. [electronic resource] by Marsh, Ashley P L Lukic, Vesna Pope, Kate Bromhead, Catherine Tankard, Rick Ryan, Monique M Yiu, Eppie M Sim, Joe C H Delatycki, Martin B Amor, David J McGillivray, George Sherr, Elliott H Bahlo, Melanie Leventer, Richard J Lockhart, Paul J Producer: 20160412 In: Neurology. Genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance. [electronic resource] by Marsh, Ashley P L Heron, Delphine Edwards, Timothy J Quartier, Angélique Galea, Charles Nava, Caroline Rastetter, Agnès Moutard, Marie-Laure Anderson, Vicki Bitoun, Pierre Bunt, Jens Faudet, Anne Garel, Catherine Gillies, Greta Gobius, Ilan Guegan, Justine Heide, Solveig Keren, Boris Lesne, Fabien Lukic, Vesna Mandelstam, Simone A McGillivray, George McIlroy, Alissandra Méneret, Aurélie Mignot, Cyril Morcom, Laura R Odent, Sylvie Paolino, Annalisa Pope, Kate Riant, Florence Robinson, Gail A Spencer-Smith, Megan Srour, Myriam Stephenson, Sarah E M Tankard, Rick Trouillard, Oriane Welniarz, Quentin Wood, Amanda Brice, Alexis Rouleau, Guy Attié-Bitach, Tania Delatycki, Martin B Mandel, Jean-Louis Amor, David J Roze, Emmanuel Piton, Amélie Bahlo, Melanie Billette de Villemeur, Thierry Sherr, Elliott H Leventer, Richard J Richards, Linda J Lockhart, Paul J Depienne, Christel Producer: 20170905 In: Nature genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)