Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine

被引：18

作者：

Li, Marilyn M. ^{[1
,2
]}

Andersson, Hans C. ^{[1
,2
]}

机构：

[1] Tulane Univ, Hayward Genet Ctr, Sch Med, New Orleans, LA 70112 USA

[2] Tulane Univ, Dept Pediat, Sch Med, New Orleans, LA 70112 USA

来源：

JOURNAL OF PEDIATRICS | 2009年 / 155卷 / 03期

关键词：

ACUTE MYELOID-LEUKEMIA; MICRODELETION SYNDROME; STRUCTURAL VARIATION; MENTAL-RETARDATION; MUTATIONS; REARRANGEMENTS; DISEASE; HYBRIDIZATION; DUPLICATION; IDENTIFICATION;

D O I：

10.1016/j.jpeds.2009.04.001

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

[No abstract available]

引用

页码：311 / 317

页数：7

共 62 条

[1] Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2 [J].

Ballif, Blake C. ;

Hornor, Sara A. ;

Jenkins, Elizabeth ;

Madan-Khetarpal, Suneeta ;

Surti, Urvashi ;

Jackson, Kelly E. ;

Asamoah, Alexander ;

Brock, Pamela L. ;

Gowans, Gordon C. ;

Conway, Robert L. ;

Graham, John M., Jr. ;

Medne, Livija ;

Zackai, Elaine H. ;

Shaikh, Tamim H. ;

Geoghegan, Joel ;

Selzer, Rebecca R. ;

Eis, Peggy S. ;

Bejjani, Bassem A. ;

Shaffer, Lisa G. .

NATURE GENETICS, 2007, 39 (09) :1071-1073

[2] Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer [J].

Bergamaschi, Anna ;

Kim, Young H. ;

Wang, Pei ;

Sorlie, Therese ;

Hernandez-Boussard, Tina ;

Lonning, Per E. ;

Tibshirani, Robert ;

Borresen-Dale, Anne-Lise ;

Pollack, Jonathan R. .

GENES CHROMOSOMES & CANCER, 2006, 45 (11) :1033-1040

[3] Whole genome oligonucleotide-based array comparative genomic hybridization analysis identified fibroblast growth factor I as a prognostic marker for advanced-stage serous ovarian adenocarcinomas [J].

Birrer, Michael J. ;

Johnson, Michael E. ;

Hao, Ke ;

Wong, Kwong-Kwok ;

Park, Dong-Choon ;

Bell, Aaron ;

Welch, William R. ;

Berkowitz, Ross S. ;

Mok, Samuel C. .

JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (16) :2281-2287

[4]

Borozdin Wiktor, 2007, Hum Mutat, V28, P830, DOI 10.1002/humu.9502

[5] Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization [J].

Brunetti-Pierri, N. ;

Grange, D. K. ;

Ou, Z. ;

Peiffer, D. A. ;

Peacock, S. K. G. ;

Cooper, M. L. ;

Eng, P. A. ;

Lalani, S. R. ;

Chinault, A. C. ;

Gunderson, K. L. ;

Craigen, W. J. ;

Cheung, S-W .

CLINICAL GENETICS, 2007, 72 (05) :411-419

[6] High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients [J].

Carrasco, DR ;

Tonon, G ;

Huang, YS ;

Zhang, YY ;

Sinha, R ;

Bin, F ;

Stewart, JP ;

Zhan, FG ;

Khatry, D ;

Protopopova, M ;

Protopopov, A ;

Sukhdeo, K ;

Hanamura, I ;

Stephens, O ;

Barlogie, B ;

Anderson, KC ;

Chin, L ;

Shaughnessy, JD ;

Brennan, C ;

DePinho, RA .

CANCER CELL, 2006, 9 (04) :313-325

[7]

CASPERSSON T, 1970, CHROMOSOMA, V30, P215

[8] Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia [J].

Crolla, JA ;

van Heyningen, V .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (05) :1138-1149

[9]

DAVENPORT SLH, 1986, CLIN GENET, V29, P298

[10]

Driscoll D. A., 1995, American Journal of Human Genetics, V57, pA33

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