نتائج البحث - Vendula Martinů

Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype–phenotype correlations حسب Johanna Raidt, Sarah Riepenhausen, Petra Pennekamp, Heike Olbrich, Israel Amirav, Rodrigo Abensur Athanazio, Micha Aviram, Juan E. Balinotti, O. Baron, Sebastian F. N. Bode, Mieke Boon, Melissa Borrelli, S.B. Carr, Suzanne Crowley, Eleonora Dehlink, Sandra Diepenhorst, Peter Ďurdík, Bernd Dworniczak, Nagehan Emiralioğlu, Ela Erdem Eralp, Rossella Fonnesu, Serena Gracci, Jörg Große-Onnebrink, Karolina Gwozdziewicz, Eric G. Haarman, C.R. Hansen, Claire Hogg, Mathias Geldermann Holgersen, Eitan Kerem, Robert Walter Körner, Karsten Kötz, Panayiotis Κouis, Michael R. Loebinger, Natalie Lorent, Jane S. Lucas, Debora Maj, Marcus Mall, June K. Marthin, Vendula Martinů, Henryk Mazurek, Hannah M. Mitchison, Tabea Nöthe-Menchen, Uğur Özçelik, Massimo Pifferi, Andrzej Pogorzelski, Felix C. Ringshausen, Jobst Roehmel, Sandra Rovira‐Amigo, Nisreen Rumman, Anne Schlegtendal, Amelia Shoemark, Synne Sperstad Kennelly, Ben O. Staar, Sivagurunathan Sutharsan, Simon Thomas, Nicola Ullmann, Julian Varghese, Sandra von Hardenberg, Woolf T. Walker, Martin Wetzke, Michał Witt, Panayiotis K. Yiallouros, Anna Zschocke, Ewa Ziętkiewicz, Kim G. Nielsen, Heymut Omran

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