Cheryl A Hill

Summary

Publications

  1. Wang Y, Sun M, Uhlhorn V, Zhou X, Peter I, Martinez Abadias N, et al. Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice. BMC Dev Biol. 2010;10:22 pubmed publisher
    ..We previously reported an inbred transgenic mouse model with the Fgfr2 +/S252W mutation on the C57BL/6J background for Apert syndrome. Here we present a mouse model for the Fgfr2+/P253R mutation...