-
1
-
-
0034129516
-
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene
-
(2000)
Nat Genet
, vol.25
, pp. 144-146
-
-
Albertson, D.G.1
Ylstra, B.2
Segraves, R.3
Collins, C.4
Dairkee, S.H.5
Kowbel, D.6
Kuo, W.L.7
Gray, J.W.8
Pinkel, D.9
-
11
-
-
0028829783
-
Inversion duplication of the short arm of chromosome 8: Clinical data on seven patients and review of the literature
-
(1995)
Am J Med Genet
, vol.59
, pp. 369-374
-
-
De Die-Smulders, C.E.1
Engelen, J.J.2
Schrander-Stumpel, C.T.3
Govaerts, L.C.4
De Vries, B.5
Vles, J.S.6
Wagemans, A.7
Schijns-Fleuren, S.8
Gillessen-Kaesbach, G.9
Fryns, J.P.10
-
12
-
-
0035083998
-
Clinical studies on submicroscopic subtelomeric rearrangements: A checklist
-
(2001)
J Med Genet
, vol.38
, pp. 145-150
-
-
De Vries, B.B.1
White, S.M.2
Knight, S.J.3
Regan, R.4
Homfray, T.5
Young, I.D.6
Super, M.7
McKeown, C.8
Splitt, M.9
Quarrell, O.W.10
Trainer, A.H.11
Niermeijer, M.F.12
Malcolm, S.13
Flint, J.14
Hurst, J.A.15
Winter, R.M.16
-
18
-
-
0030960829
-
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 1-8
-
-
Knight, S.J.1
Horsley, S.W.2
Regan, R.3
Lawrie, N.M.4
Maher, E.J.5
Cardy, D.L.6
Flint, J.7
Kearney, L.8
-
19
-
-
0033851883
-
An optimized set of human telomere clones for studying telomere integrity and architecture
-
(2000)
Am J Hum Genet
, vol.67
, pp. 320-332
-
-
Knight, S.J.1
Lese, C.M.2
Precht, K.S.3
Kuc, J.4
Ning, Y.5
Lucas, S.6
Regan, R.7
Brenan, M.8
Nicod, A.9
Lawrie, N.M.10
Cardy, D.L.11
Nguyen, H.12
Hudson, T.J.13
Riethman, H.C.14
Ledbetter, D.H.15
Flint, J.16
-
20
-
-
0033552424
-
Subtle chromosomal rearrangements in children with unexplained mental retardation
-
(1999)
Lancet
, vol.354
, pp. 1676-1681
-
-
Knight, S.J.1
Regan, R.2
Nicod, A.3
Horsley, S.W.4
Kearney, L.5
Homfray, T.6
Winter, R.M.7
Bolton, P.8
Flint, J.9
-
22
-
-
16044371402
-
A complete set of human telomeric probes and their clinical application
-
(1996)
Nat Genet
, vol.14
, pp. 86-89
-
-
Ning, Y.1
Roschke, A.2
Smith, A.C.M.3
Macha, M.4
Precht, K.5
Riethman, H.6
Ledbetter, D.H.7
Flint, J.8
Horsley, S.9
Regan, R.10
Kearney, L.11
Knight, S.12
Kvaloy, K.13
Brown, W.R.A.14
-
23
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
Dairkee, S.H.11
Ljung, B.M.12
Gray, J.W.13
Albertson, D.G.14
-
25
-
-
0032852132
-
A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis
-
(1999)
Genes Chromosomes Cancer
, vol.26
, pp. 115-124
-
-
Simons, A.1
Schepens, M.2
Forus, A.3
Godager, L.4
Van Asseldonk, M.5
Myklebost, O.6
Van Kessel, A.G.7
-
27
-
-
0032901062
-
Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres
-
(1999)
J Med Genet
, vol.36
, pp. 405-411
-
-
Slavotinek, A.1
Rosenberg, M.2
Knight, S.3
Gaunt, L.4
Fergusson, W.5
Killoran, C.6
Clayton-Smith, J.7
Kingston, H.8
Campbell, R.H.9
Flint, J.10
Donnai, D.11
Biesecker, L.12
-
28
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
Law, S.11
Myambo, K.12
Palmer, J.13
Ylstra, B.14
Yue, J.P.15
Gray, J.W.16
Jain, A.N.17
Pinkel, D.18
Albertson, D.G.19
-
29
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
32
-
-
0036173663
-
Array based comparative genomic hybridization for the differential diagnosis of renal cell cancer
-
(2002)
Cancer Res
, vol.62
, pp. 957-960
-
-
Wilhelm, M.1
Veltman, J.A.2
Olshen, A.3
Jain, A.4
Moore, D.H.5
Kovacs, G.6
Presti, J.C.7
Waldman, F.M.8
|