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
2000; Springer Science+Business Media; Volume: 106; Issue: 3 Linguagem: Inglês
10.1007/s004390000246
ISSN1432-1203
AutoresThilo Dörk, Milan Maçek, Frauke Mekus, Burkhard Tümmler, J. Tzountzouris, Teresa Casals, Alice Krebsová, Monika Koudová, Iva Sakmaryová, Milan Maçek, V. Vávrová, D. Zemková, E. K. Ginter, Н.В. Петрова, T. Ivaschenko, В. С. Баранов, Michał Witt, Andrzej Pogorzelski, Jerzy Bal, C. Zékanowsky, Klaus Wagner, Manfred Stuhrmann, Ingrid Bauer, H. H. Seydewitz, Thomas Neumann, S. Jakubiczka, Cornelia Kraus, B. Thamm, M. Nechiporenko, Л. А. Лившиц, Н И Моссэ, G L Tsukerman, Ľudevít Kádaši, Metka Ravnik‐Glavač, Damjan Glavač, Radovan Komel, Katja Vouk, Vaidutis Kučinskas, Astrīda Krūmiņa, M. Teder, Светлана Кочева, Г. Д. Ефремов, Tuncer Onay, Betül Kırdar, Geraldine Malone, M. Schwarz, Zhaoqing Zhou, K.J. Friedman, Sophie Carles, M. Claustres, Dominique Bozon, C. Verlingue, Claude Férec, Maria Tzetis, Emmanouel Kanavakis, H. Cuppens, C. Bombieri, П. Ф. Пигнатти, Federica Sangiuolo, Albena Jordanova, Jelena Kušić‐Tišma, Dragica Radojković, Jadranka Sertić, Darko Richter, Ana Stavljenić-Rukavina, Erik Björck, Birgitta Strandvik, H. Cardoso, Mark Montgomery, Barbara E.M. Nakielna, Daniel Hughes, Xavier Estivill, Isabel Aznarez, Elizabeth Tullis, L.-C. Tsui, Julian Zielenski,
Tópico(s)Congenital Ear and Nasal Anomalies
Referência(s)