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Noethe-Menchen, Tabea, Wallmeier, Julia, Pennekamp, Petra, Hoeben, Inga M., Olbrich, Heike, Loges, Niki T., Raidt, Johanna, Dougherty, Gerard W., Hjeij, Rim, Dworniczak, Bernd, Omran, Heymut, Amirav, Israel, Biebach, Luisa, Fabricius, Dorit, Griese, Matthias, Grosse-Onnebrink, Joerg, Haeffner, Karsten, Hector, Andreas, Jung, Andreas, Kaiser-Labusch, Petra, Kaiser, Thomas, Kessler, Christina, Kitz, Richard, Knowles, Michael R., Koerner-Rettberg, Cordula, Kristoffersson, Ulf, Leigh, Margaret W., Mertsch, Pontus, Mischo, Bernhard, Nielsen, Kim G., Poeta, Marco ORCID: 0000-0002-7515-1394, Rietschel, Ernst, Roth, Samra, Santamaria, Francesca, Schmalstieg, Christian, Schmidts, Miriam, Schwarz, Carsten, Schwerk, Nicolaus, Seithe, Horst, Tebbe, Johannes, Werner, Claudius and Zariwala, Maimoona A. (2019). Randomization of Left-Right Asymmetry and Congenital Heart Defects The Role of DNAH5 in Humans and Mice. Circ.-Genom. Precis. Med., 12 (11). PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 2574-8300
Veit, Christof, Bierbaum, Thomas, Wesselmann, Simone, Stock, Stephanie, Heidecke, Claus-Dieter, Apfelbacher, Christian, Benz, Stefan, Dreinhoefer, Karsten E., Hauptmann, Michael ORCID: 0000-0001-8539-0148, Hoffmann, Falk, Hoffmann, Wolfgang, Kaiser, Thomas, Klinkhammer-Schalke, Monika, Koller, Michael, Kostuj, Tanja, Ortmann, Olaf, Schmitt, Jochen, Schuenemann, Holger and Geraedts, Max . Routine Practice Data for Health Care Analyses: Part 3 of the Manual. Gesundheitswesen. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-4421
Vervoelgyi, Elke, Kromp, Mandy, Skipka, Guido, Bender, Ralf and Kaiser, Thomas (2011). Reporting of loss to follow-up information in randomised controlled trials with time-to-event outcomes: a literature survey. BMC Med. Res. Methodol., 11. LONDON: BMC. ISSN 1471-2288
Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Noethe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas ORCID: 0000-0002-6699-0014, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhan B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmueller, Janine, Krenz, Henrike, Woeste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J. and Omran, Heymut (2019). De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. Am. J. Hum. Genet., 105 (5). S. 1030 - 1040. CAMBRIDGE: CELL PRESS. ISSN 1537-6605