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Citation: Sw. Horsley et al., Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects, EUR J HUM G, 9(3), 2001, pp. 217-225

Authors: Daniels, RJ Peden, JF Lloyd, C Horsley, SW Clark, K Tufarelli, C Kearney, L Buckle, VJ Doggett, NA Flint, J Higgs, DR

Citation: Rj. Daniels et al., Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16, HUM MOL GEN, 10(4), 2001, pp. 339-352

Authors: Ogilvie, CM Harrison, RH Horsley, SW Hodgson, SV Kearney, L

Citation: Cm. Ogilvie et al., A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?, CYTOG C GEN, 92(1-2), 2001, pp. 69-73

Authors: Brown, J Horsley, SW Jung, C Saracoglu, K Janssen, B Brough, M Daschner, M Beedgen, B Kerkhoffs, G Eils, R Harris, PC Jauch, A Kearney, L

Citation: J. Brown et al., Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL, EUR J HUM G, 8(12), 2000, pp. 903-910

Authors: Speleman, F Callens, B Logghe, K Van Roy, N Horsley, SW Jauch, A Verschraegen-Spae, MR Leroy, JG

Citation: F. Speleman et al., Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35 -> qter: Molecular cytogenetic analysis and clinical phenotype intwo generations, AM J MED G, 93(5), 2000, pp. 349-354

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