Authors:
de Vries, BBA
Bitner-Glindzicz, M
Knight, SJL
Tyson, J
MacDermot, KD
Flint, J
Malcolm, S
Winter, RM
Citation: Bba. De Vries et al., A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome, CLIN GENET, 58(6), 2000, pp. 483-487
Authors:
Knight, SJL
Lese, CM
Precht, KS
Kuc, J
Ning, Y
Lucas, S
Regan, R
Brenan, M
Nicod, A
Lawrie, NM
Cardy, DLN
Nguyen, H
Hudson, TJ
Riethman, HC
Ledbetter, DH
Flint, J
Citation: Sjl. Knight et al., An optimized set of human telomere clones for studying telomere integrity and architecture, AM J HU GEN, 67(2), 2000, pp. 320-332
Citation: J. Flint, The English in West Africa, 1681-1683: The local correspondence of the Royal African Company of England, 1681-1699, part 1, INT HIST R, 21(2), 1999, pp. 479-480
Citation: Kj. Brackley et al., A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation, PRENAT DIAG, 19(6), 1999, pp. 570-574
Authors:
Knight, SJL
Regan, R
Nicod, A
Horsley, SW
Kearney, L
Homfray, T
Winter, RM
Bolton, P
Flint, J
Citation: Sjl. Knight et al., Subtle chromosomal rearrangements in children with unexplained mental retardation, LANCET, 354(9191), 1999, pp. 1676-1681
Authors:
Slavotinek, A
Rosenberg, M
Knight, S
Gaunt, L
Fergusson, W
Killoran, C
Clayton-Smith, J
Kingston, H
Campbell, RHA
Flint, J
Donnai, D
Biesecker, L
Citation: A. Slavotinek et al., Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosometelomeres, J MED GENET, 36(5), 1999, pp. 405-411