2012 – August / ENGLISH
V. Laugel-Haushalter, A. Langer, J. Marrie, V. Fraulob, B. Schuhbaur, M. Koch-Phillips, P. Dollé, A. Bloch-Zupan
Orodental anomalies are one aspect of rare diseases and are increasingly identified as diagnostic and predictive traits. To understand the rationale behind gene expression during tooth or other ectodermal derivative development and the disruption of odontogenesis or hair and salivary gland formation in human syndromes we analyzed the expression patterns of a set of genes (Irf6, Nfkbia, Ercc3, Evc2, Map2k1) involved in human ectodermal dysplasias in mouse by in situ hybridization. […]