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	1.	The non-neurologists' view on epilepsy syndromes classification. [electronic resource] by Vears, D F Grinton, B E Producer: 20060829 In: Epileptic disorders : international epilepsy journal with videotape vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	2.	How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis. [electronic resource] by Vears, D F Niemiec, E Howard, H C Borry, P Producer: 20191028 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Action myoclonus-renal failure syndrome: a cause for worsening tremor in young adults. [electronic resource] by Vadlamudi, L Vears, D F Hughes, A Pedagogus, E Berkovic, S F Producer: 20061108 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Reply to Kranendonk et al. [electronic resource] by Sénécal, K Thys, K Vears, D F Van Assche, K Knoppers, B M Borry, P Producer: 20171130 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsy. [electronic resource] by Tan, N C K Heron, S E Scheffer, I E Pelekanos, J T McMahon, J M Vears, D F Mulley, J C Berkovic, S F Producer: 20050518 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Points to consider for laboratories reporting results from diagnostic genomic sequencing. [electronic resource] by Vears, D F Sénécal, K Clarke, A J Jackson, L Laberge, A M Lovrecic, L Piton, A Van Gassen, K L I Yntema, H G Knoppers, B M Borry, P Producer: 20181211 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure. [electronic resource] by Dibbens, L M Michelucci, R Gambardella, A Andermann, F Rubboli, G Bayly, M A Joensuu, T Vears, D F Franceschetti, S Canafoglia, L Wallace, R Bassuk, A G Power, D A Tassinari, C A Andermann, E Lehesjoki, A E Berkovic, S F Producer: 20091117 In: Annals of neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)