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2018
Montalbano, A., Juergensen, L., Roeth, R., Weiss, B., Fukami, M., Fricke-Otto, S., Binder, G., Ogata, T., Decker, E., Nuernberg, G., Hassel, D. and Rappold, G. (2018). Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. Eur. J. Hum. Genet., 26. S. 217 - 218. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438
Schneider, S., Riessland, M., Kaczmarek, A., Swoboda, K. J., Loehr, H., Bradler, C., Grysko, V., Dimitriadi, M., Hosseinibarkooie, S., Torres-Benito, L., Peters, M., Upadhyay, A., Biglari, N., Kroeber, S., Hoelker, I., Garbes, L., Gilissen, C., Hoischen, A., Nuernberg, G., Nuernberg, P., Walter, M., Rigo, F., Bennett, C. F., Kye, M. J., Hart, A. C., Hammerschmidt, M., Kloppenburg, P. and Wirth, B. (2018). Neurocalcin delta as a novel protective modifier for spinal muscular atrophy: A full story from gene identification to therapy. Eur. J. Hum. Genet., 26. S. 55 - 57. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438
2017
Ahmad, I., Baig, S. M., Abdulkareem, A. R., Hussain, M. S., Sur, I., Toliat, M. R., Nuernberg, G., Dalibor, N., Moawia, A., Waseem, S. S., Asif, M., Nagra, H., Sher, M., Khan, M. M. A., Hassan, I., Rehman, S. Ur, Thiele, H., Altmueller, J., Noegel, A. A. and Nuernberg, P. (2017). Genetic heterogeneity in Pakistani microcephaly families revisited. Clin. Genet., 92 (1). S. 62 - 69. HOBOKEN: WILEY. ISSN 1399-0004
2015
Hessler, N., Geise, M. H., I, Coassin, S., Moskau-Hartmannt, S., Nuernberg, G., Hennig, F., Bauer, M., Moehlenkamp, S., Mahabadi, A. A., Moebus, S., Erbel, R., Karl-Heinz, J., Hoffmann, B., Nuemberg, P., Klockgether, T., Kronenberg, F., Scherag, A. and Ziegler, A. (2015). Linkage and Association Analyses of Carotid Intima Media Thickness for Common Genomic Variants: Results from the Bonn IMT Family Study and The Heinz Nixdorf Recall Study. Hum. Hered., 79 (1). S. 37 - 38. BASEL: KARGER. ISSN 1423-0062