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Jump to: 2018 | 2017 | 2015
Number of items: 4.

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

This list was generated on Sat Apr 17 01:32:37 2021 CEST.