-
1
-
-
0141994858
-
Genomic microarrays in human genetic disease and cancer
-
Albertson DG, Pinkel D (2003) Genomic microarrays in human genetic disease and cancer. Hum Mol Genet Spec No 12:R145-R152
-
(2003)
Hum Mol Genet Spec No
, vol.12
-
-
Albertson, D.G.1
Pinkel, D.2
-
2
-
-
0035143677
-
Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization
-
Bell KA, Van Deerlin PG, Feinberg RF, du Manoir S, Haddad BR (2001) Diagnosis of aneuploidy in archival, paraffin-embedded pregnancy-loss tissues by comparative genomic hybridization. Fertil Steril 75:374-379
-
(2001)
Fertil Steril
, vol.75
, pp. 374-379
-
-
Bell, K.A.1
Van Deerlin, P.G.2
Feinberg, R.F.3
Du Manoir, S.4
Haddad, B.R.5
-
3
-
-
0032953537
-
Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading
-
Bell KA, Van Deerlin PG, Haddad BR, Feinberg RF (1999) Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading. Fertil Steril 71:334-341
-
(1999)
Fertil Steril
, vol.71
, pp. 334-341
-
-
Bell, K.A.1
Van Deerlin, P.G.2
Haddad, B.R.3
Feinberg, R.F.4
-
4
-
-
0036218046
-
Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays
-
Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A (2002) Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays. Nat Biotechnol 20:393-396
-
(2002)
Nat Biotechnol
, vol.20
, pp. 393-396
-
-
Cai, W.W.1
Mao, J.H.2
Chow, C.W.3
Damani, S.4
Balmain, A.5
Bradley, A.6
-
5
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook EH Jr, Lindgren V, Leventhal BL, Courchesne R, Lincoln A, Shulman C, Lord C, Courchesne E (1997) Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 60:928-934
-
(1997)
Am J Hum Genet
, vol.60
, pp. 928-934
-
-
Cook Jr., E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
Lord, C.7
Courchesne, E.8
-
6
-
-
0031839349
-
Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization
-
Daniely M, Aviram-Goldring A, Barkai G, Goldman B (1998) Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization. Hum Reprod 13:805-809
-
(1998)
Hum Reprod
, vol.13
, pp. 805-809
-
-
Daniely, M.1
Aviram-Goldring, A.2
Barkai, G.3
Goldman, B.4
-
7
-
-
17844397183
-
Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH): Re-evaluation of chromosome aberration rates in early spontaneous abortions
-
Fritz B, Hallermann C, Olert J, Fuchs B, Bruns M, Aslan M, Schmidt S, Coerdt W, Muntefering H, Rehder H (2001) Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH): re-evaluation of chromosome aberration rates in early spontaneous abortions. Eur J Hum Genet 9:539-547
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 539-547
-
-
Fritz, B.1
Hallermann, C.2
Olert, J.3
Fuchs, B.4
Bruns, M.5
Aslan, M.6
Schmidt, S.7
Coerdt, W.8
Muntefering, H.9
Rehder, H.10
-
9
-
-
10744226995
-
Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q
-
Gunn SR, Mohammed M, Reveles XT, Viskochil DH, Palumbos JC, Johnson-Pais TL, Hale DE, Lancaster JL, Hardies LJ, Boespflug-Tanguy O, Cody JD, Leach RJ (2003) Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q. Am J Med Genet 120A: 127-135
-
(2003)
Am J Med Genet
, vol.120 A
, pp. 127-135
-
-
Gunn, S.R.1
Mohammed, M.2
Reveles, X.T.3
Viskochil, D.H.4
Palumbos, J.C.5
Johnson-Pais, T.L.6
Hale, D.E.7
Lancaster, J.L.8
Hardies, L.J.9
Boespflug-Tanguy, O.10
Cody, J.D.11
Leach, R.J.12
-
10
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
Hassold T, Chen N, Funkhouser J, Jooss T, Manuel B, Matsuura J, Matsuyama A, Wilson C, Yamane JA, Jacobs PA (1980) A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet 44:151-178
-
(1980)
Ann Hum Genet
, vol.44
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
Jooss, T.4
Manuel, B.5
Matsuura, J.6
Matsuyama, A.7
Wilson, C.8
Yamane, J.A.9
Jacobs, P.A.10
-
11
-
-
18344392245
-
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas
-
Hodgson G, Hager JH, Volik S, Hariono S, Wernick M, Moore D, Nowak N, Albertson DG, Pinkel D, Collins C, Hanahan D, Gray JW (2001) Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas. Nat Genet 29:459-464
-
(2001)
Nat Genet
, vol.29
, pp. 459-464
-
-
Hodgson, G.1
Hager, J.H.2
Volik, S.3
Hariono, S.4
Wernick, M.5
Moore, D.6
Nowak, N.7
Albertson, D.G.8
Pinkel, D.9
Collins, C.10
Hanahan, D.11
Gray, J.W.12
-
12
-
-
0026495364
-
Comparative genomic hybridization: A powerful new method for cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F, Pinkel D (1992) Comparative genomic hybridization: a powerful new method for cytogenetic analysis of solid tumors. Science 258:818-821
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
Pinkel, D.7
-
13
-
-
0041823216
-
Ring 21 chromosome and a satellited 1p in the same patient: Novel origin for an ectopic NOR
-
Ki A, Rauen KA, Black LD, Kostiner DR, Sandberg PL, Pinkel D, Albertson DG, Norton ME, Cotter PD (2003) Ring 21 chromosome and a satellited 1p in the same patient: novel origin for an ectopic NOR. Am J Med Genet 120A:365-369
-
(2003)
Am J Med Genet
, vol.120 A
, pp. 365-369
-
-
Ki, A.1
Rauen, K.A.2
Black, L.D.3
Kostiner, D.R.4
Sandberg, P.L.5
Pinkel, D.6
Albertson, D.G.7
Norton, M.E.8
Cotter, P.D.9
-
14
-
-
0034754559
-
High resolution comparative genomic hybridisation in clinical cytogenetics
-
Kirchhoff M, Rose H, Lundsteen C (2001) High resolution comparative genomic hybridisation in clinical cytogenetics. J Med Genet 38:740-744
-
(2001)
J Med Genet
, vol.38
, pp. 740-744
-
-
Kirchhoff, M.1
Rose, H.2
Lundsteen, C.3
-
15
-
-
0033926516
-
Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions
-
Lomax B, Tang S, Separovic E, Phillips D, Hillard E, Thomson T, Kalousek DK (2000) Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions. Am J Hum Genet 66:1516-1521
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1516-1521
-
-
Lomax, B.1
Tang, S.2
Separovic, E.3
Phillips, D.4
Hillard, E.5
Thomson, T.6
Kalousek, D.K.7
-
16
-
-
0037370718
-
High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization in genomic microarrays
-
Paris PL, Albertson DG, Alers JC, Andaya A, Carroll P, Fridlyand J, Jain AN, Kamkar S, Kowbel D, Krijtenburg PJ, Pinkel D, Schroder FH, Vissers KJ, Watson VJ, Wildhagen MF, Collins C, Van Dekken H (2003) High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization in genomic microarrays. Am J Pathol 162:763-770
-
(2003)
Am J Pathol
, vol.162
, pp. 763-770
-
-
Paris, P.L.1
Albertson, D.G.2
Alers, J.C.3
Andaya, A.4
Carroll, P.5
Fridlyand, J.6
Jain, A.N.7
Kamkar, S.8
Kowbel, D.9
Krijtenburg, P.J.10
Pinkel, D.11
Schroder, F.H.12
Vissers, K.J.13
Watson, V.J.14
Wildhagen, M.F.15
Collins, C.16
Van Dekken, H.17
-
17
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, Collins C, Kuo WL, Chen C, Zhai Y, Dairkee SH, Ljung BM, Gray JW, Albertson DG (1998) High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211
-
(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
-
18
-
-
0038150493
-
DNA microarray analysis in malignant lymphomas
-
Schwaenen C, Wessendorf S, Kestler HA, Dohner H, Lichter P, Bentz M (2003) DNA microarray analysis in malignant lymphomas. Ann Hematol 82:323-332
-
(2003)
Ann Hematol
, vol.82
, pp. 323-332
-
-
Schwaenen, C.1
Wessendorf, S.2
Kestler, H.A.3
Dohner, H.4
Lichter, P.5
Bentz, M.6
-
19
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B, Kimura K, Law S, Myambo K, Palmer J, Ylstra B, Yue JP, Gray JW, Jain AN, Pinkel D, Albertson DG (2001) Assembly of microarrays for genome-wide measurement of DNA copy number. Nat Genet 29:263-264
-
(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
-
20
-
-
0034842667
-
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies
-
Tabet AC, Aboura A, Dauge MC, Audibert F, Coulomb A, Batallan A, Couturier-Turpin MH, Feldmann G, Tachdjian G (2001) Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies. Prenat Diagn 21:613-618
-
(2001)
Prenat Diagn
, vol.21
, pp. 613-618
-
-
Tabet, A.C.1
Aboura, A.2
Dauge, M.C.3
Audibert, F.4
Coulomb, A.5
Batallan, A.6
Couturier-Turpin, M.H.7
Feldmann, G.8
Tachdjian, G.9
-
21
-
-
18344379676
-
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization
-
Veltman JA, Schoenmakers EFPM, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, van Kessel AG (2002) High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization. Am J Hum Genet 70: 1269-1276
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1269-1276
-
-
Veltman, J.A.1
Schoenmakers, E.F.P.M.2
Eussen, B.H.3
Janssen, I.4
Merkx, G.5
Van Cleef, B.6
Van Ravenswaaij, C.M.7
Brunner, H.G.8
Smeets, D.9
Van Kessel, A.G.10
-
22
-
-
9144240478
-
Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities
-
Vissers LELM, de Vries BBA, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EHLPG, van Rijk A, Smeets D, van Ravenswaaij-Arts CMA, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, van Kessel AG, Schoenmakers EFPM, Veltman JA (2003) Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities. Am J Hum Genet 73:1261-1270
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1261-1270
-
-
Vissers, L.E.L.M.1
De Vries, B.B.A.2
Osoegawa, K.3
Janssen, I.M.4
Feuth, T.5
Choy, C.O.6
Straatman, H.7
Van Der Vliet, W.8
Huys, E.H.L.P.G.9
Van Rijk, A.10
Smeets, D.11
Van Ravenswaaij-Arts, C.M.A.12
Knoers, N.V.13
Van Der Burgt, I.14
De Jong, P.J.15
Brunner, H.G.16
Van Kessel, A.G.17
Schoenmakers, E.F.P.M.18
Veltman, J.A.19
|