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	41.	HLA-DRB1 and month of birth in multiple sclerosis. [electronic resource] by Ramagopalan, S V Link, J Byrnes, J K Dyment, D A Giovannoni, G Hintzen, R Q Sundqvist, E Kockum, I Smestad, C Lie, B A Harbo, H F Padyukov, L Alfredsson, L Olsson, T Sadovnick, A D Hillert, J Ebers, G C Producer: 20100108 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families. [electronic resource] by Hartley, T Wagner, J D Warman-Chardon, J Tétreault, M Brady, L Baker, S Tarnopolsky, M Bourque, P R Parboosingh, J S Smith, C McInnes, B Innes, A M Bernier, F Curry, C J Yoon, G Horvath, G A Bareke, E Gillespie, M Majewski, J Bulman, D E Dyment, D A Boycott, K M Producer: 20190730 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencing. [electronic resource] by Balci, T B Hartley, T Xi, Y Dyment, D A Beaulieu, C L Bernier, F P Dupuis, L Horvath, G A Mendoza-Londono, R Prasad, C Richer, J Yang, X-R Armour, C M Bareke, E Fernandez, B A McMillan, H J Lamont, R E Majewski, J Parboosingh, J S Prasad, A N Rupar, C A Schwartzentruber, J Smith, A C Tétreault, M Innes, A M Boycott, K M Producer: 20180430 In: Clinical genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Genetic susceptibility to MS: a second stage analysis in Canadian MS families. [electronic resource] by Dyment, D A Willer, C J Scott, B Armstrong, H Ligers, A Hillert, J Paty, D W Hashimoto, S Devonshire, V Hooge, J Kastrukoff, L Oger, J Metz, L Warren, S Hader, W Power, C Auty, A Nath, A Nelson, R Freedman, M Brunet, D Paulseth, J E Rice, G O'Connor, P Duquette, P Lapierre, Y Francis, G Bouchard, J P Murray, T J Bhan, V Maxner, C Pryse-Phillips, W Stefanelli, M Sadovnick, A D Risch, N Ebers, G C Producer: 20020116 In: Neurogenetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management. [electronic resource] by Avila, M Dyment, D A Sagen, J V St-Onge, J Moog, U Chung, B H Y Mo, S Mansour, S Albanese, A Garcia, S Martin, D O Lopez, A A Claudi, T König, R White, S M Sawyer, S L Bernstein, J A Slattery, L Jobling, R K Yoon, G Curry, C J Merrer, M L Luyer, B L Héron, D Mathieu-Dramard, M Bitoun, P Odent, S Amiel, J Kuentz, P Thevenon, J Laville, M Reznik, Y Fagour, C Nunes, M-L Delesalle, D Manouvrier, S Lascols, O Huet, F Binquet, C Faivre, L Rivière, J-B Vigouroux, C Njølstad, P R Innes, A M Thauvin-Robinet, C Publication details: Clinical genetics Apr 2016 In: Clinical genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care. [electronic resource] by Sawyer, S L Hartley, T Dyment, D A Beaulieu, C L Schwartzentruber, J Smith, A Bedford, H M Bernard, G Bernier, F P Brais, B Bulman, D E Warman Chardon, J Chitayat, D Deladoëy, J Fernandez, B A Frosk, P Geraghty, M T Gerull, B Gibson, W Gow, R M Graham, G E Green, J S Heon, E Horvath, G Innes, A M Jabado, N Kim, R H Koenekoop, R K Khan, A Lehmann, O J Mendoza-Londono, R Michaud, J L Nikkel, S M Penney, L S Polychronakos, C Richer, J Rouleau, G A Samuels, M E Siu, V M Suchowersky, O Tarnopolsky, M A Yoon, G Zahir, F R Majewski, J Boycott, K M Producer: 20161213 In: Clinical genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)