AAAAAA

   
Results: 1-7 |
Results: 7
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects
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
A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals
Authors: Elanko, N Sibbring, JS Metcalfe, KA 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
A high bandwidth interface for haptic human computer interaction
Authors: Wall, SA Harwin, W
Citation: Sa. Wall et W. Harwin, A high bandwidth interface for haptic human computer interaction, MECHATRONIC, 11(4), 2001, pp. 371-387
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
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
A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?
Authors: Johnson, D Wall, SA Mann, S Wilkie, AOM
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
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome
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
De novo Alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
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
Risultati: 1-7 |