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Naslov Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice (Review)
Autori Castellani C Cuppens H Macek M Jr Cassinian JJ Kerern E Durie P Tullis E Assael BM Bombieri C Brown A Casals T Claustres M Cutting GR Dequeker Elisabeth MC Dodge J Doull I Farrell P Ferec C Girodon Emmanuelle Johannesson M Kerem B Knowles M Munck A Pignatti PF Radojkovic Dragica P Rizzotti P Schwarz M Stuhnnann M Tzetis M Zielenski J Elborn JS 
Info JOURNAL OF CYSTIC FIBROSIS, (2008), vol. 7 br. 3, str. 179-196
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis (Article)
Autori Radivojevic Danijela  Djurisic Marina Lalic Tanja Guc-Scekic Marija P Savic Jovan Minic Predrag B Antoniadi T Tzetis M Kanavakis E 
Info GENETIC TESTING, (2004), vol. 8 br. 3, str. 276-280
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov 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 (Article)
Autori Dork T Macek M Mekus F Tummler B Tzountzouris J Casals T Krebsova A Koudova M Sakmaryova I Macek M Vavrova V Zemkova D Ginter E Petrova NV Ivaschenko T Baranov V Witt M Pogorzelski A Bal J Zekanowsky C Wagner K Stuhrmann M Bauer I Seydewitz HH Neumann T Jakubiczka S Kraus C Thamm B Nechiporenko M Livshits LA Mosse N Tsukerman G Kadasi Ludevit Ravnik-Glavac M Glavac D Komel R Vouk K Kucinskas V Krumina A Teder M Kocheva S Efremov GD Onay T Kirdar B Malone G Schwarz M Zhou ZQ Friedman KJ Carles S Claustres M Bozon D Verlingue C Ferec C Tzetis M Kanavakis E Cuppens H Bombieri C Pignatti PF Sangiuolo F Jordanova Albena Kusic Jelena S  Radojkovic Dragica P Sertic Jadranka Richter D Rukavina-Stavljenic Ana Bjorck E Strandvik B Cardoso H Montgomery M Nakielna B Hughes D Estivill X Aznarez I Tullis E Tsui LC Zielenski J 
Info HUMAN GENETICS, (2000), vol. 106 br. 3, str. 259-268
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