-
1
-
-
0034129516
-
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene
-
Albertson DG, Ylstra B, Segraves R, Collins C, Dairkee SH, Kowbel D, Kuo WL, Gray JW, Pinkel D (2000) Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene. Nat Genet 25:144-146
-
(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
-
2
-
-
33646046176
-
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization
-
Ballif BC, Kashork CD, Saleki R, Rorem E, Sundin K, Bejjani BA, Shaffer LG (2006) Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization. Prenat Diagn 26:333-339
-
(2006)
Prenat Diagn
, vol.26
, pp. 333-339
-
-
Ballif, B.C.1
Kashork, C.D.2
Saleki, R.3
Rorem, E.4
Sundin, K.5
Bejjani, B.A.6
Shaffer, L.G.7
-
3
-
-
27144547761
-
Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro
-
Benkhalifa M, Kasakyan1 S, Clement P, Baldi M, Tachdjian G, Demirol A, Gurgan T, Fiorentino F, Mohammed M, Qumsiyeh MB (2005) Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro. Prenat Diagn 25:894-900
-
(2005)
Prenat Diagn
, vol.25
, pp. 894-900
-
-
Benkhalifa, M.1
Kasakyan, S.2
Clement, P.3
Baldi, M.4
Tachdjian, G.5
Demirol, A.6
Gurgan, T.7
Fiorentino, F.8
Mohammed, M.9
Qumsiyeh, M.B.10
-
4
-
-
0035252636
-
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
-
Bruder CE, Hirvela C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang XX, Evans DG, Wallace AJ, Baser ME, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Rask-Andersen H, Kluwe L, Mautner V, Sainio M, Hung G, Mathiesen T, Moller C, Pulst SM, Harder H, Heiberg A, Honda M, Niimura M, Sahlen S, Blennow E, Albertson DG, Pinkel D, Dumanski JP (2001) High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Hum Mol Genet 10:271-282
-
(2001)
Hum Mol Genet
, vol.10
, pp. 271-282
-
-
Bruder, C.E.1
Hirvela, C.2
Tapia-Paez, I.3
Fransson, I.4
Segraves, R.5
Hamilton, G.6
Zhang, X.X.7
Evans, D.G.8
Wallace, A.J.9
Baser, M.E.10
Zucman-Rossi, J.11
Hergersberg, M.12
Boltshauser, E.13
Papi, L.14
Rouleau, G.A.15
Poptodorov, G.16
Jordanova, A.17
Rask-Andersen, H.18
Kluwe, L.19
Mautner, V.20
Sainio, M.21
Hung, G.22
Mathiesen, T.23
Moller, C.24
Pulst, S.M.25
Harder, H.26
Heiberg, A.27
Honda, M.28
Niimura, M.29
Sahlen, S.30
Blennow, E.31
Albertson, D.G.32
Pinkel, D.33
Dumanski, J.P.34
more..
-
5
-
-
0014234658
-
Chemical differentiation along metaphase chromosomes
-
Caspersson T, Farber S, Foley GE, Kudynowski J, Modest EJ, Simonsson E, Wagh U, Zech L (1968) Chemical differentiation along metaphase chromosomes. Exp Cell Res 49:219-222
-
(1968)
Exp Cell Res
, vol.49
, pp. 219-222
-
-
Caspersson, T.1
Farber, S.2
Foley, G.E.3
Kudynowski, J.4
Modest, E.J.5
Simonsson, E.6
Wagh, U.7
Zech, L.8
-
6
-
-
23744491866
-
Development and validation of a CGH microarray for clinical cytogenetic diagnosis
-
Cheung SW, Shaw CA, Yu W, Li J, Ou Z, Patel A, Yatsenko SA, Cooper ML, Furman P, Stankiewicz P, Lupski JR, Chinault AC, Beaudet AL (2005) Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genet Med 7:422-432
-
(2005)
Genet Med
, vol.7
, pp. 422-432
-
-
Cheung, S.W.1
Shaw, C.A.2
Yu, W.3
Li, J.4
Ou, Z.5
Patel, A.6
Yatsenko, S.A.7
Cooper, M.L.8
Furman, P.9
Stankiewicz, P.10
Lupski, J.R.11
Chinault, A.C.12
Beaudet, A.L.13
-
7
-
-
28044448703
-
Array comparative genomic hybridization analysis of uterine leiomyosarcoma
-
Cho YL, Bae SM, Koo MS, Kim KM, Chun HJ, Kim CK, Ro DY, Kim JH, Lee CH, Kim YW, Ahn WS (2005) Array comparative genomic hybridization analysis of uterine leiomyosarcoma. Gynecol Oncol 99:545-551
-
(2005)
Gynecol Oncol
, vol.99
, pp. 545-551
-
-
Cho, Y.L.1
Bae, S.M.2
Koo, M.S.3
Kim, K.M.4
Chun, H.J.5
Kim, C.K.6
Ro, D.Y.7
Kim, J.H.8
Lee, C.H.9
Kim, Y.W.10
Ahn, W.S.11
-
8
-
-
33846681527
-
Characterization of supernumerary chromosomal markers: A study of 13 casaes
-
Douet-Guilbert N, Marical H, Pinson L, Herry A, Le Bris MJ, Morel F, De Braekeleer M (2007) Characterization of supernumerary chromosomal markers: a study of 13 casaes. Cytogenet Genome Res 116:18-23
-
(2007)
Cytogenet Genome Res
, vol.116
, pp. 18-23
-
-
Douet-Guilbert, N.1
Marical, H.2
Pinson, L.3
Herry, A.4
Le Bris, M.J.5
Morel, F.6
De Braekeleer, M.7
-
9
-
-
0030943279
-
Construction of a bacterial artificial chromosome library containing large EcoRI and Hind III genomic fragments of lettuce
-
Frijters ACJ, Zhang Z, van Damme M, Wang G-L, Ronald PC, Michelmore RW (1997) Construction of a bacterial artificial chromosome library containing large EcoRI and Hind III genomic fragments of lettuce. Theor Appl Genet 94:390-399
-
(1997)
Theor Appl Genet
, vol.94
, pp. 390-399
-
-
Frijters, A.C.J.1
Zhang, Z.2
Van Damme, M.3
Wang, G.-L.4
Ronald, P.C.5
Michelmore, R.W.6
-
10
-
-
0031741317
-
Klinefelter's syndrome as a model of anomalous cerebral laterality: Testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray
-
Geschwind DH, Gregg J, Boone K, Karrim J, Pawlikowska-Haddal A, Rao E, Ellison J, Ciccodicola A, D'Urso M, Woods R, Rappold GA, Swerdloff R, Nelson SF (1998) Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray. Dev Genet 23:215-229
-
(1998)
Dev Genet
, vol.23
, pp. 215-229
-
-
Geschwind, D.H.1
Gregg, J.2
Boone, K.3
Karrim, J.4
Pawlikowska-Haddal, A.5
Rao, E.6
Ellison, J.7
Ciccodicola, A.8
D'Urso, M.9
Woods, R.10
Rappold, G.A.11
Swerdloff, R.12
Nelson, S.F.13
-
11
-
-
27444441193
-
Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization
-
Hayashi S, Kurosawa K, Imoto I, Mizutani S, Inazawa J (2005) Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization. Am J Med Genet 139A:32-36
-
(2005)
Am J Med Genet
, vol.139
, pp. 32-36
-
-
Hayashi, S.1
Kurosawa, K.2
Imoto, I.3
Mizutani, S.4
Inazawa, J.5
-
12
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C (2004) Detection of large-scale variation in the human genome. Nat Genet 36:949-951
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
14
-
-
10744233914
-
A tiling resolution DNA microarray with complete coverage of the human genome
-
Ishkanian AS, Malloff CA, Watson SK, DeLeeuw RJ, Chi B, Coe BP, Snijders A, Albertson DG, Pinkel D, Marra MA, Ling V, MacAulay C, Lam WL (2004) A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet 36:299-303
-
(2004)
Nat Genet
, vol.36
, pp. 299-303
-
-
Ishkanian, A.S.1
Malloff, C.A.2
Watson, S.K.3
Deleeuw, R.J.4
Chi, B.5
Coe, B.P.6
Snijders, A.7
Albertson, D.G.8
Pinkel, D.9
Marra, M.A.10
Ling, V.11
MacAulay, C.12
Lam, W.L.13
-
15
-
-
34247171671
-
Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis
-
Jardim A, Melo JB, Matoso E, Pires LM, Ramos L, Carreira IM (2007) Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis. Prenat Diagn 27:380-381
-
(2007)
Prenat Diagn
, vol.27
, pp. 380-381
-
-
Jardim, A.1
Melo, J.B.2
Matoso, E.3
Pires, L.M.4
Ramos, L.5
Carreira, I.M.6
-
16
-
-
4344625842
-
Small supernumerary marker chromosomes (sSMC) in humans
-
Liehr T, Claussen U, Starke H (2004) Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 107:55-67
-
(2004)
Cytogenet Genome Res
, vol.107
, pp. 55-67
-
-
Liehr, T.1
Claussen, U.2
Starke, H.3
-
17
-
-
27644520395
-
Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation
-
Liehr T, Mrasek K, Weise A, Dufke A, Rodriguez L, Guardia NM, Sanchis A, Vermeesch JR, Ramel C, Polityko A, Haas OA, Anderson J, Claussen U, Eggeling F, Starke H (2006) Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation. Cytogenet Genome Res 112:23-34
-
(2006)
Cytogenet Genome Res
, vol.112
, pp. 23-34
-
-
Liehr, T.1
Mrasek, K.2
Weise, A.3
Dufke, A.4
Rodriguez, L.5
Guardia, N.M.6
Sanchis, A.7
Vermeesch, J.R.8
Ramel, C.9
Polityko, A.10
Haas, O.A.11
Anderson, J.12
Claussen, U.13
Eggeling, F.14
Starke, H.15
-
18
-
-
33750555572
-
Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype
-
Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ (2006) Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype. Prenat Diagn 26:898-902
-
(2006)
Prenat Diagn
, vol.26
, pp. 898-902
-
-
Lin, C.C.1
Hsieh, Y.Y.2
Wang, C.H.3
Li, Y.C.4
Hsieh, L.J.5
Lee, C.C.6
Tsai, C.H.7
Tsai, F.J.8
-
19
-
-
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
-
20
-
-
10744231187
-
Representational oligonucleotide microarray analysis: A high-resolution method to detect genome copy number variation
-
Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M, Rodgers L, Brady A, Sebat J, Troge J, West JA, Rostan S, Nguyen KC, Powers S, Ye KQ, Olshen A, Venkatraman E, Norton L, Wigler M (2003) Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. Genome Res 13:2291-2305
-
(2003)
Genome Res
, vol.13
, pp. 2291-2305
-
-
Lucito, R.1
Healy, J.2
Alexander, J.3
Reiner, A.4
Esposito, D.5
Chi, M.6
Rodgers, L.7
Brady, A.8
Sebat, J.9
Troge, J.10
West, J.A.11
Rostan, S.12
Nguyen, K.C.13
Powers, S.14
Ye, K.Q.15
Olshen, A.16
Venkatraman, E.17
Norton, L.18
Wigler, M.19
-
21
-
-
1442280674
-
DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets
-
Mantripragada KK, Tapia-Paez I, Blennow E, Nilsson P, Wedell A, Dumanski JP (2004) DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets. Int J Mol Med 13:273-279
-
(2004)
Int J Mol Med
, vol.13
, pp. 273-279
-
-
Mantripragada, K.K.1
Tapia-Paez, I.2
Blennow, E.3
Nilsson, P.4
Wedell, A.5
Dumanski, J.P.6
-
22
-
-
33744979546
-
Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid
-
Miura S, Miura K, Masuzaki H, Miyake N, Yoshiura K, Sosonkina N, Harada N, Shimokawa O, Nakayama D, Yoshimura S, Matsumoto N, Niikawa N, Ishimaru T (2006) Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid. J Hum Genet 51:412-417
-
(2006)
J Hum Genet
, vol.51
, pp. 412-417
-
-
Miura, S.1
Miura, K.2
Masuzaki, H.3
Miyake, N.4
Yoshiura, K.5
Sosonkina, N.6
Harada, N.7
Shimokawa, O.8
Nakayama, D.9
Yoshimura, S.10
Matsumoto, N.11
Niikawa, N.12
Ishimaru, T.13
-
23
-
-
33645983981
-
Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array
-
Park SJ, Jeong SY, Kim HJ (2006) Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array. Cancer Genet Cytogenet 166:56-64
-
(2006)
Cancer Genet Cytogenet
, vol.166
, pp. 56-64
-
-
Park, S.J.1
Jeong, S.Y.2
Kim, H.J.3
-
24
-
-
0022446922
-
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
-
Pinkel D, Straume T, Gray JW (1986) Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 83:2934-2938
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
25
-
-
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
-
26
-
-
33645778232
-
Prenatal detection of unbalanced chromosomal rearrangements by array CGH
-
Rickman L, Fiegler H, Shaw-Smith C, Nash R, Cirigliano V, Voglino G, Ng BL, Scott C, Whittaker J, Adinolfi M, Carter NP, Bobrow M (2006) Prenatal detection of unbalanced chromosomal rearrangements by array CGH. J Med Genet 43:353-361
-
(2006)
J Med Genet
, vol.43
, pp. 353-361
-
-
Rickman, L.1
Fiegler, H.2
Shaw-Smith, C.3
Nash, R.4
Cirigliano, V.5
Voglino, G.6
Ng, B.L.7
Scott, C.8
Whittaker, J.9
Adinolfi, M.10
Carter, N.P.11
Bobrow, M.12
-
27
-
-
33751172713
-
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization
-
Sahoo T, Cheung SW, Ward P, Darilek S, Patel A, Gaudio D, Kang SH, Lalani SR, Li J, McAdoo S, Burke A, Shaw CA, Stankiewicz P, Chinault AC, Veyver IB, Roa BB, Beaudet AL, Eng CM (2006) Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med 8:719-727
-
(2006)
Genet Med
, vol.8
, pp. 719-727
-
-
Sahoo, T.1
Cheung, S.W.2
Ward, P.3
Darilek, S.4
Patel, A.5
Gaudio, D.6
Kang, S.H.7
Lalani, S.R.8
Li, J.9
McAdoo, S.10
Burke, A.11
Shaw, C.A.12
Stankiewicz, P.13
Chinault, A.C.14
Veyver, I.B.15
Roa, B.B.16
Beaudet, A.L.17
Eng, C.M.18
-
28
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Maner S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, Reiner A, Gilliam TC, Trask B, Patterson N, Zetterberg A, Wigler M (2004) Large-scale copy number polymorphism in the human genome. Science 305:525-528
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
Navin, N.11
Lucito, R.12
Healy, J.13
Hicks, J.14
Ye, K.15
Reiner, A.16
Gilliam, T.C.17
Trask, B.18
Patterson, N.19
Zetterberg, A.20
Wigler, M.21
more..
-
29
-
-
2942575149
-
A cytogeneticist's perspective on genomic microarrays
-
Shaffer LG, Bejjani BA (2004) A cytogeneticist's perspective on genomic microarrays. Hum Reprod Update 10:221-226
-
(2004)
Hum Reprod Update
, vol.10
, pp. 221-226
-
-
Shaffer, L.G.1
Bejjani, B.A.2
-
30
-
-
0034513406
-
Molecular mechanisms for constitutional chromosomal rearrangements in humans
-
Shaffer LG, Lupski JR (2000) Molecular mechanisms for constitutional chromosomal rearrangements in humans. Annu Rev Genet 34:297-329
-
(2000)
Annu Rev Genet
, vol.34
, pp. 297-329
-
-
Shaffer, L.G.1
Lupski, J.R.2
-
31
-
-
33746167778
-
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases
-
Shaffer LG, Kashork CD, Saleki R, Rorem E, Sundin K, Ballif BC, Bejjani BA (2006) Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases. J Pediatr 149:98-102
-
(2006)
J Pediatr
, vol.149
, pp. 98-102
-
-
Shaffer, L.G.1
Kashork, C.D.2
Saleki, R.3
Rorem, E.4
Sundin, K.5
Ballif, B.C.6
Bejjani, B.A.7
-
32
-
-
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
-
33
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T, Lichter P (1997) Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer 20:399-407
-
(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
-
34
-
-
20044362567
-
Molecular karyotyping: Array CGH quality criteria for constitutional genetic diagnosis
-
Vermeesch JR, Melotte C, Froyen G, Van Vooren S, Dutta B, Maas N, Vermeulen S, Menten B, Speleman F, De Moor B, Van Hummelen P, Marynen P, Fryns JP, Devriendt K (2005) Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis. J Histochem Cytochem 53:413-422
-
(2005)
J Histochem Cytochem
, vol.53
, pp. 413-422
-
-
Vermeesch, J.R.1
Melotte, C.2
Froyen, G.3
Van Vooren, S.4
Dutta, B.5
Maas, N.6
Vermeulen, S.7
Menten, B.8
Speleman, F.9
De Moor, B.10
Van Hummelen, P.11
Marynen, P.12
Fryns, J.P.13
Devriendt, K.14
-
35
-
-
9144240478
-
Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities
-
Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO, Straatman H, van der Vliet W, Huys EH, van Rijk A, Smeets D, van Ravenswaaij-Arts CM, Knoers NV, van der Burgt I, de Jong PJ, Brunner HG, van Kessel AG, Schoenmakers EF, 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.1
De Vries, B.B.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.9
Van Rijk, A.10
Smeets, D.11
Van Ravenswaaij-Arts, C.M.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.18
Veltman, J.A.19
-
36
-
-
10744221541
-
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
-
Yu W, Ballif BC, Kashork CD, Heilstedt HA, Howard LA, Cai WW, White LD, Liu W, Beaudet AL, Bejjani BA, Shaw CA, Shaffer LG (2003) Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions. Hum Mol Genet 12:2145-2152
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2145-2152
-
-
Yu, W.1
Ballif, B.C.2
Kashork, C.D.3
Heilstedt, H.A.4
Howard, L.A.5
Cai, W.W.6
White, L.D.7
Liu, W.8
Beaudet, A.L.9
Bejjani, B.A.10
Shaw, C.A.11
Shaffer, L.G.12
|