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	1.	ERCC6 founder mutation identified in Finnish patients with COFS syndrome. [electronic resource] by Jaakkola, E Mustonen, A Olsen, P Miettinen, S Savuoja, T Raams, A Jaspers, N G J Shao, H Wu, B L Ignatius, J Producer: 20110222 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaks. [electronic resource] by Niedernhofer, Laura J Odijk, Hanny Budzowska, Magda van Drunen, Ellen Maas, Alex Theil, Arjan F de Wit, Jan Jaspers, N G J Beverloo, H Berna Hoeijmakers, Jan H J Kanaar, Roland Producer: 20040804 In: Molecular and cellular biology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome. [electronic resource] by Oh, Kyu-Seon Khan, Sikandar G Jaspers, N G J Raams, Anja Ueda, Takahiro Lehmann, Alan Friedmann, Peter S Emmert, Steffen Gratchev, Alexi Lachlan, Katherine Lucassan, Anneke Baker, Carl C Kraemer, Kenneth H Producer: 20061207 In: Human mutation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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