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Journal Article
Ellerbroek, V. L., Bonfig, W., Doerr, H. -G., Bettendorf, M., Hauffa, B., Fricke-Otto, S., Rohrer, T., Reschke, F., Schoenau, E., Schwab, K. O., Kapelari, K., Roehl, F. -W., Mohnike, K. and Holl, R. W. (2015). Long-term Surveillance of Children with Congenital Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (AQUAPE Hypo Dok). Klinische Padiatr., 227 (4). S. 199 - 206. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3824
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