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	Title	Author(s)	Issue Date
	Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: A cystic fibrosis mutation of Slavic origin common in Central and East Europe Journal:Human Genetics	Dörk, T Macek Jr, M Mekus, F Tümmler, B Tzountzouris, J Casals, T Krebsová, A Koudová, M Sakmaryová, I Macek Sr, M Vávrová, V Zemková, D Ginter, E Petrova, NV Ivaschenko, T Baranov, V Witt, M Pogorzelski, A Bal, J Zékanowsky, C Wagner, K Stuhrmann, M Bauer, I Seydewitz, HH Neumann, T Jakubiczka, S Kraus, C Thamm, B Nechiporenko, M Livshits, L Mosse, N Tsukerman, G Kadási, L RavnikGlavač, M Glavač, D Komel, R Vouk, K Kučinskas, V Krumina, A Teder, M Kocheva, S Efremov, GD Onay, T Kirdar, B Malone, G Schwarz, M Zhou, Z Friedman, KJ Carles, S Claustres, M Bozon, D Verlingue, C Férec, C Tzetis, M Kanavakis, E Cuppens, H Bombieri, C Pignatti, PF Sangiuolo, F Jordanova, A Kusic, J Radojkovič, D Sertić, J Richter, D Rukavina, AS Bjorck, E Strandvik, B Cardoso, H Montgomery, M Nakielna, B Hughes, D Estivill, X Aznarez, I Tullis, E Tsui, LC Zielenski, J	2000
	Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families Journal:Human Genetics	Dork, T Neumann, T Wulbrand, U Wulf, B Kalin, N Maass, G Krawczak, M Guillermit, H Ferec, C Horn, G Klinger, K Kerem, BS Zielenski, J Tsui, LC Tummler, B	1992

Showing results 1 to 2 of 2