Idiopathic learning disability and genome imbalance. by Knight, S, Regan, R

New and emerging treatments for estrogen receptor-positive breast cancer: focus on everolimus by Paplomata E, O'Regan R

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Human subtelomeric probes: applications in practice by Kearney, L, Knight, S, Horsley, S, Regan, R, Flint, J

Detection of two chromosomal arrangements in the subtelomeric region of 9q in mentally retarded children. by Nokelainen, P, Quarrell, O, Kerr, B, Regan, R, Flint, J

Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition. by Regan, R, Smith, K, Crocker, M, Guiver, C, Taylor, J, Knight, S

Introduction of array CGH into the clinical setting: The Oxford Laboratory experience by Crocker, M, Candlin, R, Connell, L, Knight, S, Regan, R, Smith, K

Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay. by Sismani, C, Armour, J, Flint, J, Girgalli, C, Regan, R, Patsalis, P

Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3. by Knight-Jones, E, Knight, S, Heussler, H, Regan, R, Flint, J, Martin, K

DOP-PCR products amplified from genomic DNA can be used reliably in whole genome array CGH studie for the detection of delections and duplications in leukaemia by Wilson, K, Ballabio, E, Regan, R, Hedman, A, Jarrett, R, Knight, S, Tosi, S

Identification of a submicroscopic familial 4p;11p translocation using multiple telomere probe FISH analysis by Knight, S, Regan, R, Flint, J, Horsley, S, Kearney, L, Temple, I, Young, I

A fluorescence in situ hybridisation (FISH) assay for submicroscopic chromosome rearrangements involving telomers. by Horsley, S, Knight, S, Regan, R, Cardy, D, Lawrie, N, Flint, J, Kearney, L

Subtelomeric rearrangements and idiopathic mental retardation by Regan, R, Knight, S, Nicod, A, Lucas, S, Horsley, S, Kearney, L, Bolton, P, Flint, J

Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. by Knight, S, Horsley, S, Regan, R, Lawrie, N, Maher, E, Cardy, D, Flint, J, Kearney, L

Wolf-Hirschhorn Syndrome: developmental outcome and mortality correlate with deletion size. by Shannon, N, Regan, R, Maltby, E, Flint, J, Rigby, A, Hall, D, Quarrell, O

Subtle chromosomal rearrangements in children with unexplained mental retardation. by Knight, S, Regan, R, Nicod, A, Horsley, S, Kearney, L, Homfray, T, Winter, R, Bolton, P, Flint, J

Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13). by de Vries, B, Lees, M, Knight, S, Regan, R, Corney, D, Flint, J, Barnicoat, A, Winter, R

Whole genome microarrays for the detection of cryptic genomic imbalances in idiopathic learning disability by Regan, R, Smith, K, Crocker, M, Hedman, A, Honey, B, Hurst, J, Taylor, J, Flint, J, Knight, S

Microarray technology in healthcare: A cost analysis in idiopathic learning disability by Wordsworth, S, Buchanan, J, Regan, R, Smith, K, Davison, V, Dyer, S, Campbell, C, Maher, E, Knight, S, Taylor, J

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom. by Wordsworth, S, Buchanan, J, Regan, R, Davison, V, Smith, K, Dyer, S, Campbell, C, Blair, E, Maher, E, Taylor, J, Knight, S

A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration. by Ning, Y, Roschke, A, Smith, A, Macha, M, Precht, K, Riethman, H, Ledbetter, D, Flint, J, Horsley, S, Regan, R, Kearney, L, Knight, S, Kvaloy, K, Brown, W