Authors:
Mavrogiannis, LA
Antonopoulou, I
Baxova, A
Kutilek, S
Kim, CA
Sugayama, SM
Salamanca, A
Wall, SA
Morriss-Kay, GM
Wilkie, AOM
Citation: La. Mavrogiannis et al., Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects, NAT GENET, 27(1), 2001, pp. 17-18
Citation: C. Hayes et Gm. Morriss-kay, Retinoic acid specifically downregulates Fgf4 and inhibits posterior cell proliferation in the developing mouse autopod, J ANAT, 198, 2001, pp. 561-568
Authors:
Johnson, D
Iseki, S
Wilkie, AOM
Morriss-Kay, GM
Citation: D. Johnson et al., Expression patterns of Twist and Fgfr1, -2 and -3 in the developing mouse coronal suture suggest a key role for Twist in suture initiation and biogenesis, MECH DEVEL, 91(1-2), 2000, pp. 341-345
Citation: S. Iseki et al., Fgfr1 and Fgfr2 have distinct differentiation- and proliferation-related roles in the developing mouse skull vault, DEVELOPMENT, 126(24), 1999, pp. 5611-5620
Authors:
Oldridge, M
Zackai, EH
McDonald-McGinn, DM
Iseki, S
Morriss-Kay, GM
Twigg, RF
Johnson, D
Wall, SA
Jiang, W
Theda, C
Jabs, EW
Wilkie, AOM
Citation: M. Oldridge et al., De novo Alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome, AM J HU GEN, 64(2), 1999, pp. 446-461