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Citation: La. Mavrogiannis et al., Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects, NAT GENET, 27(1), 2001, pp. 17-18
Authors:
Elanko, N
Sibbring, JS
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Clayton-Smith, J
Donnai, D
Temple, IK
Wall, SA
Wilkie, AOM
Citation: N. Elanko et al., A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals, HUM MUTAT, 18(6), 2001, pp. 535-541
Authors:
Wilkie, AOM
Tang, ZQ
Elanko, N
Walsh, S
Twigg, SRF
Hurst, JA
Wall, SA
Chrzanowska, KH
Maxson, RE
Citation: Aom. Wilkie et al., Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification, NAT GENET, 24(4), 2000, pp. 387-390
Citation: D. Johnson et al., A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?, EUR J HUM G, 8(8), 2000, pp. 571-577
Authors:
Glaser, RL
Jiang, W
Boyadjiev, SA
Tran, AK
Zachary, AA
Van Maldergem, L
Johnson, M
Walsh, S
Oldridge, M
Wall, SA
Wilkie, AOM
Jabs, EW
Citation: Rl. Glaser et al., Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome, AM J HU GEN, 66(3), 2000, pp. 768-777
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