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Journal of Medical Genetics|September 11, 1998
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangementsS W Horsley, S J Knight, J Nixon, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 1998
Rapid mapping of markers applying vectorette technology to YAC fragmentation allows easy assembly of a high-density STS bacterial clone contig spanning the markers D6S1260-D6S1918J D Shearman, J J Pointon, A T Merryweather-Clarke, et al.
Human Molecular Genetics|August 1, 1996
Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elementsJ Flint, J Rochette, C F Craddock, et al.
Health Technology Assessment (Winchester, England)|July 2, 2009
Cetuximab plus radiotherapy for the treatment of locally advanced squamous cell carcinoma of the head and neckS Griffin, S Walker, M Sculpher, et al.
Health Technology Assessment (Winchester, England)|July 2, 2009
The use of paclitaxel in the management of early stage breast cancerS Griffin, G Dunn, S Palmer, et al.
Genes, Chromosomes & Cancer|August 31, 2004
Comparative expressed sequence hybridization studies of high-hyperdiploid childhood acute lymphoblastic leukemiaAlicja M Gruszka-Westwood, Sharon W Horsley, Angel Martinez-Ramirez, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
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-TELJ Brown, S W Horsley, C Jung, et al.
Human Molecular Genetics|February 7, 2001
Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16R J Daniels, J F Peden, C Lloyd, et al.
Genes, Chromosomes & Cancer|October 22, 2008
Covert preleukemia driven by MLL gene fusionJan Zuna, Tatiana Burjanivova, Ester Mejstrikova, et al.
American Journal of Human Genetics|October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1D Johnson, S W Horsley, D M Moloney, et al.
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