Translocation between chromosome 5q35 and chromosome 11q13 – an unusual cytogenetic finding in a primary refractory acute myeloid leukemia.

Autor: Wang, T.-F.¹, Horsley, S. W.², Lee, K.-F.³, Chu, S.-C.¹, Li, C.-C.¹, Kao, R.-H.¹ rueyhokao@tzuchi.org.tw

Publikováno v: Clinical & Laboratory Haematology. Jun2006, Vol. 28 Issue 3, p160-163. 4p.

Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements.

Autor: Flint, J., Rochette, J., Craddock, C. F., Dodé, C., Vignes, B., Horsley, S. W., Kearney, L., Buckle, V. J., Ayyub, H., Higgs, D. R.

Publikováno v: Human Molecular Genetics; Aug1996, Vol. 5 Issue 8, p1163-1169, 7p

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Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects.

Autor: Horsley SW; MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK., Daniels RJ, Anguita E, Raynham HA, Peden JF, Villegas A, Vickers MA, Green S, Waye JS, Chui DH, Ayyub H, MacCarthy AB, Buckle VJ, Gibbons RJ, Kearney L, Higgs DR

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2001 Mar; Vol. 9 (3), pp. 217-25.

A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?

Autor: Mackie Ogilvie C; Division of Medical and Molecular Genetics, King's, Guy's and St. Thomas' Medical School, London, UK. caroline.ogilvie@kcl.ac.uk, Harrison RH, Horsley SW, Hodgson SV, Kearney L

Publikováno v: Cytogenetics and cell genetics [Cytogenet Cell Genet] 2001; Vol. 92 (1-2), pp. 69-73.