Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation... von Shaw-Smith, C, Redon, R, Rickman, L, Rio, M, Willatt, L, Fiegler, H, Firth, H, Sanlaville, D, Winter, R, Colleaux, L, Bobrow, M, Carter, N P

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders von Jacquemont, M-L, Sanlaville, D, Redon, R, Raoul, O, Cormier-Daire, V, Lyonnet, S, Amiel, J, Le Merrer, M, Heron, D, de Blois, M-C, Prieur, M, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Philippe, A

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The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes von Gribble, S M, Prigmore, E, Burford, D C, Porter, K M, Ng, Bee Ling, Douglas, E J, Fiegler, H, Carr, P, Kalaitzopoulos, D, Clegg, S, Sandstrom, R, Temple, I K, Youings, S A, Thomas, N S, Dennis, N R, Jacobs, P A, Crolla, J A, Carter, N P

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Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents von Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna-Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi-Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J

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Prenatal detection of unbalanced chromosomal rearrangements by array CGH von Rickman, L, Fiegler, H, Shaw-Smith, C, Nash, R, Cirigliano, V, Voglino, G, Ng, B L, Scott, C, Whittaker, J, Adinolfi, M, Carter, N P, Bobrow, M

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Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes von Howarth, K D, Blood, K A, Ng, B L, Beavis, J C, Chua, Y, Cooke, S L, Raby, S, Ichimura, K, Collins, V P, Carter, N P, Edwards, P A W

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Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH von ICHIMURA, K, MUNGALL, A. J, FIEGLER, H, PEARSON, D. M, DUNHAM, I, CARTER, N. P, COLLINS, V. Peter

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Integration of cytogenetic landmarks into the draft sequence of the human genome von Trask, B. J, BAC Resource Consortium, The, Cheung, V. G, Nowak, N, Jang, W, Kirsch, I. R, Zhao, S, Chen, X.-N, Furey, T. S, Kim, U.-J, Kuo, W.-L, Olivier, M, Conroy, J, Kasprzyk, A, Massa, H, Yonescu, R, Sait, S, Thoreen, C, Snijders, A, Lemyre, E, Bailey, J. A, Bruzel, A, Burrill, W. D, Clegg, S. M, Collins, S, Dhami, P, Friedman, C, Han, C. S, Herrick, S, Lee, J, Ligon, A. H, Lowry, S, Morley, M, Narasimhan, S, Osoegawa, K, Peng, Z, Plajzer-Frick, I, Quade, B. J, Scott, D, Sirotkin, K, Thorpe, A. A, Gray, J. W, Hudson, J, Pinkel, D, Ried, T, Rowen, L, Shen-Ong, G. L, Strausberg, R. L, Birney, E, Callen, D. F, Cheng, J.-F, Cox, D. R, Doggett, N. A, Carter, N. P, Eichler, E. E, Haussler, D, Korenberg, J. R, Morton, C. C, Albertson, D, Schuler, G, de Jong, P. J

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Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays von Fiegler, H, Gribble, S M, Burford, D C, Carr, P, Prigmore, E, Porter, K M, Clegg, S, Crolla, J A, Dennis, N R, Jacobs, P, Carter, N P

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A DNA damage checkpoint response in telomere-initiated senescence von Fagagna, Fabrizio d'Adda di, Jackson, Stephen P, Reaper, Philip M, Clay-Farrace, Lorena, Fiegler, Heike, Carr, Philippa, von Zglinicki, Thomas, Saretzki, Gabriele, Carter, Nigel P

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Chromatin Architecture of the Human Genome: Gene-Rich Domains Are Enriched in Open Chromatin Fibers von Gilbert, Nick, Boyle, Shelagh, Fiegler, Heike, Woodfine, Kathryn, Carter, Nigel P., Bickmore, Wendy A.

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DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders von SWAMINATHAN, Ganesh J, BRAGIN, Eugene, CHATZIMICHALI, Eleni A, CORPAS, Manuel, BEVAN, A. Paul, WRIGHT, Caroline F, CARTER, Nigel P, HURLES, Matthew E, FIRTH, Helen V

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NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome von Borck, G, Redon, R, Sanlaville, D, Rio, M, Prieur, M, Lyonnet, S, Vekemans, M, Carter, N P, Munnich, A, Colleaux, L, Cormier-Daire, V

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An SNP map of human chromosome 22 von Bentley, D. R, Mullikin, J. C, Hunt, S. E, Cole, C. G, Mortimore, B. J, Rice, C. M, Burton, J, Matthews, L. H, Pavitt, R, Plumb, R. W, Sims, S. K, Ainscough, R. M. R, Attwood, J, Bailey, J. M, Barlow, K, Bruskiewich, R. M. M, Butcher, P. N, Carter, N. P, Chen, Y, Clee, C. M, Coggill, P. C, Davies, J, Davies, R. M, Dawson, E, Francis, M. D, Joy, A. A, Lamble, R. G, Langford, C. F, Macarthy, J, Mall, V, Moreland, A, Overton-Larty, E. K, Ross, M. T, Smith, L. C, Steward, C. A, Sulston, J. E, Tinsley, E. J, Turney, K. J, Willey, D. L, Wilson, G. D, McMurray, A. A, Dunham, I, Rogers, J

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Reciprocal Chromosome Painting Reveals Detailed Regions of Conserved Synteny between the Karyotypes of the Domestic Dog (Canis familiaris) and Human von Breen, Matthew, Thomas, Rachael, Binns, Matthew M., Carter, Nigel P., Langford, Cordelia F.

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Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer von Telenius, Ha˚kan, Carter, Nigel P., Bebb, Charlotte E., Nordenskjo¨ld, Magnus, Ponder, Bruce A.J., Tunnacliffe, Alan

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Ultra-high resolution array painting facilitates breakpoint sequencing von Gribble, S M, Kalaitzopoulos, D, Burford, D C, Prigmore, E, Selzer, R R, Ng, B L, Matthews, N S W, Porter, K M, Curley, R, Lindsay, S J, Baptista, J, Richmond, T A, Carter, N P

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Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or “deletion with positional effect” syndrome? von Redon, R, Rio, M, Gregory, S G, Cooper, R A, Fiegler, H, Sanlaville, D, Banerjee, R, Scott, C, Carr, P, Langford, C, Cormier-Daire, V, Munnich, A, Carter, N P, Colleaux, L

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Applications of genomic microarrays to explore human chromosome structure and function von Carter, Nigel P., Vetrie, David

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Prenatal Diagnosis by Array-CGH von Rickman, L., Fiegler, H., Carter, N.P., Bobrow, M.

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