 | Up a level |
2020
Hoelzel, S., Ishorst, N., Greve, C., Degenhardt, F., Drichel, D., Maj, C., Nothnagel, M. 
ORCID: 0000-0001-8305-7114, Hehir-Kwa, J. Y., Veltman, J. A., Kruse, T., Reutter, H., Nowak, S., Carels, C., van Rooij, I., Ludwig, K. U. and Mangold, E.
(2020).
Nonsyndromic orofacial clefts - Identifying putative causative genes by CNV analysis of whole exome sequencing data.
Eur. J. Hum. Genet., 28 (SUPPL 1).
S. 839 - 840.
LONDON:
SPRINGERNATURE.
ISSN 1476-5438
2017
Hoebel, A. K., Drichel, D., van de Vorst, M., Boehmer, A. C., Sivalingam, S., Ishorst, N., Klamt, J., Goelz, L., Alblas, M., Maaser, A., Keppler, K., Zink, A. M., Dixon, M. J., Dixon, J., Hemprich, A., Kruse, T., Graf, I., Dunsche, A., Schmidt, G., Daratsianos, N., Nowak, S., Aldhorae, K. A., Noethen, M. M., Knapp, M., Thiele, H., Gilissen, C., Reutter, H., Hoischen, A., Mangold, E. and Ludwig, K. U. (2017). Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing. J. Dent. Res., 96 (11). S. 1314 - 1322. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591
2014
Ludwig, K. U., Boehmer, A. C., Rubini, M., Mossey, P. A., Herms, S., Nowak, S., Reutter, H., Alblas, M. A., Lippke, B., Barth, S., Paredes-Zenteno, M., Munoz-Jimenez, S. G., Ortiz-Lopez, R., Kreusch, T., Hemprich, A., Martini, M., Braumann, B., Jaeger, A., Poetzsch, B., Molloy, A., Peterlin, B., Hoffmann, P., Noethen, M. M., Rojas-Martinez, A., Knapp, M., Steegers-Theunissen, R. P. and Mangold, E. (2014). Strong Association of Variants around FOXE1 and Orofacial Clefting. J. Dent. Res., 93 (4). S. 376 - 382. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591