Authors:
de Vries, BBA
White, SM
Knight, SJL
Regan, R
Homfray, T
Young, ID
Super, M
McKeown, C
Splitt, M
Quarrell, OWJ
Trainer, AH
Niermeijer, MF
Malcolm, S
Flint, J
Hurst, JA
Winter, RM
Citation: Bba. De Vries et al., Clinical studies on submicroscopic subtelomeric rearrangements: a checklist, J MED GENET, 38(3), 2001, pp. 145-150
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
Authors:
Lynch, SA
Hall, K
Precious, S
Wilkie, AOM
Hurst, JA
Citation: Sa. Lynch et al., Two further cases of Sener syndrome: frontonasal dysplasia and dilated Virchow-Robin spaces, J MED GENET, 37(6), 2000, pp. 466-470
Citation: Ja. Hurst et Ij. Wassell, Double differentially demodulated scheme for short burst OFDM systems operating in frequency selective environments, ELECTR LETT, 36(18), 2000, pp. 1559-1560
Authors:
Lai, CSL
Fisher, SE
Hurst, JA
Levy, ER
Hodgson, S
Fox, M
Jeremiah, S
Povey, S
Jamison, DC
Green, ED
Vargha-Khadem, F
Monaco, AP
Citation: Csl. Lai et al., The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder, AM J HU GEN, 67(2), 2000, pp. 357-368