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Number of items: 4.

Journal Article

Wenzel, Andrea, Altmueller, Janine, Ekici, Arif B., Popp, Bernt ORCID: 0000-0002-3679-1081, Stueber, Kurt, Thiele, Holger, Pannes, Alois, Staubach, Simon, Salido, Eduardo ORCID: 0000-0001-9599-9854, Nuernberg, Peter, Reinhardt, Richard ORCID: 0000-0001-9376-2132, Reis, Andre ORCID: 0000-0002-6301-6363, Rump, Patrick, Hanisch, Franz-Georg, Wolf, Matthias T. F., Wiesener, Michael, Huettel, Bruno and Beck, Bodo B. (2018). Single molecule real time sequencing in ADTKD-MUC1 allows complete assembly of the VNTR and exact positioning of causative mutations. Sci Rep, 8. LONDON: NATURE PUBLISHING GROUP. ISSN 2045-2322

Cartolano, Maria ORCID: 0000-0001-9830-988X, Huettel, Bruno, Hartwig, Benjamin, Reinhardt, Richard ORCID: 0000-0001-9376-2132 and Schneeberger, Korbinian (2016). cDNA Library Enrichment of Full Length Transcripts for SMRT Long Read Sequencing. PLoS One, 11 (6). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Acevedo-Garcia, Johanna, Collins, Nicholas C., Ahmadinejad, Nahal, Ma, Lu ORCID: 0000-0001-5271-0686, Houben, Andreas ORCID: 0000-0003-3419-239X, Bednarek, Pawel ORCID: 0000-0002-3064-7775, Benjdia, Mariam ORCID: 0000-0003-1554-5452, Freialdenhoven, Andreas, Altmueller, Janine, Nuernberg, Peter, Reinhardt, Richard ORCID: 0000-0001-9376-2132, Schulze-Lefert, Paul and Panstruga, Ralph ORCID: 0000-0002-3756-8957 (2013). Fine mapping and chromosome walking towards the Ror1 locus in barley (Hordeum vulgare L.). Theor. Appl. Genet., 126 (12). S. 2969 - 2983. NEW YORK: SPRINGER. ISSN 1432-2242

Olbrich, Heike, Schmidts, Miriam ORCID: 0000-0002-1714-6749, Werner, Claudius, Onoufriadis, Alexandros, Loges, Niki T., Raidt, Johanna, Banki, Nora Fanni, Shoemark, Amelia ORCID: 0000-0001-7360-6060, Burgoyne, Tom, Al Turki, Saeed, Hurles, Matthew E., Koehler, Gabriele, Schroeder, Josef, Nuernberg, Gudrun, Nuernberg, Peter, Chung, Eddie M. K., Reinhardt, Richard ORCID: 0000-0001-9376-2132, Marthin, June K., Nielsen, Kim G., Mitchison, Hannah M. and Omran, Heymut (2012). Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry. Am. J. Hum. Genet., 91 (4). S. 672 - 685. CAMBRIDGE: CELL PRESS. ISSN 1537-6605

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