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	1.	SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. [electronic resource] by Hannibal, M C Ruzzo, E K Miller, L R Betz, B Buchan, J G Knutzen, D M Barnett, K Landsverk, M L Brice, A LeGuern, E Bedford, H M Worrall, B B Lovitt, S Appel, S H Andermann, E Bird, T D Chance, P F Producer: 20090601 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. [electronic resource] by Collie, A M B Landsverk, M L Ruzzo, E Mefford, H C Buysse, K Adkins, J R Knutzen, D M Barnett, K Brown, R H Parry, G J Yum, S W Simpson, D A Olney, R K Chinnery, P F Eichler, E E Chance, P F Hannibal, M C Producer: 20101215 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity. [electronic resource] by Bachmann-Gagescu, R Dempsey, J C Phelps, I G O'Roak, B J Knutzen, D M Rue, T C Ishak, G E Isabella, C R Gorden, N Adkins, J Boyle, E A de Lacy, N O'Day, D Alswaid, A Ramadevi A, Radha Lingappa, L Lourenço, C Martorell, L Garcia-Cazorla, À Ozyürek, H Haliloğlu, G Tuysuz, B Topçu, M Chance, P Parisi, M A Glass, I A Shendure, J Doherty, D Producer: 20160505 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)