Authors: Hajihosseini, MK Wilson, S De Moerlooze, L Dickson, C

Citation: Mk. Hajihosseini et al., A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes, P NAS US, 98(7), 2001, pp. 3855-3860

Authors: Revest, JM Spencer-Dene, B Kerr, K De Moerlooze, L Rosewell, I Dickson, C

Citation: Jm. Revest et al., Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 andis required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4, DEVELOP BIO, 231(1), 2001, pp. 47-62

Authors: De Moerlooze, L Spencer-Dene, B Revest, JM Hajihosseini, M Rosewell, I Dickson, C

Citation: L. De Moerlooze et al., An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis, DEVELOPMENT, 127(3), 2000, pp. 483-492

Authors: De Moerlooze, L Williamson, J Liners, F Perret, J Parmentier, M

Citation: L. De Moerlooze et al., Cloning and chromosomal mapping of the mouse and human genes encoding the orphan glucocorticoid-induced receptor (GPR83), CYTOG C GEN, 90(1-2), 2000, pp. 146-150