Items where Author is "Burdine, Rebecca D."

2012

Panizzi, Jennifer R. and Becker-Heck, Anita and Castleman, Victoria H. and Al-Mutairi, Dalal A. and Liu, Yan and Loges, Niki T. and Pathak, Narendra and Austin-Tse, Christina and Sheridan, Eamonn and Schmidts, Miriam and Olbrich, Heike and Werner, Claudius and Häffner, Karsten and Hellman, Nathan and Chodhari, Rahul and Gupta, Amar and Kramer-Zucker, Albrecht and Olale, Felix and Burdine, Rebecca D. and Schier, Alexander F. and O'Callaghan, Christopher and Chung, Eddie M. K. and Reinhardt, Richard and Mitchison, Hannah M. and King, Stephen M. and Omran, Heymut and Drummond, Iain A.. (2012) CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms. Nature Genetics, 44 (6). pp. 714-719.

2005

Dutta, Sunit and Dietrich, Jens-Erik and Aspöck, Gudrun and Burdine, Rebecca D. and Schier, Alexander and Westerfield, Monte and Varga, Zoltán M.. (2005) pitx3 defines an equivalence domain for lens and anterior pituitary placode. Development, 132 (7). pp. 1579-1590.

2002

de la Cruz, June M. and Bamford, Richard N. and Burdine, Rebecca D. and Roessler, Erich and Barkovich, James A. and Donnai, Dian and Schier, Alexander F. and Muenke, Maximilian. (2002) A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects. Human genetics, 110 (5). pp. 422-428.