INVITED AND SPECIAL SESSIONS
Thursday, October 27
2:00 PM-4:30 PM
Concurrent Platform Sessions II (33-39) Click on abstract number to view full text
SESSION 33 - Array CGH: Clinical Diagnosis and Gene Identification
Hall E
Co-Moderators: Art Brothman, University of Utah School of Medicine, Salt Lake City; and Charles Lee, Brigham & Women's Hospital, Boston, MA
77/2:00 A targeted chromosomal microarray for CGH-based analysis of clinically relevant chromosomal disorders and subtelomeric regions. S. Cheung, C. Shaw, J. Li, Z. Ou, A. Patel, E. Brundage, S. Yatsenko, L. Cooper, S. Trilochan, P. Ward, P. Stankiewicz, W. Cai, J. Lupski, C. Chinault and A. Beaudet.
78/2:15 Identification of cytogenetic abnormalities by microarray analysis: a study of 1,300 consecutive clinical cases. L. G. Shaffer, C. D. Kashork, B. C. Ballif and B. A. Bejjani.
79/2:30 Array-MAPH: A novel microarray technology for genomic analysis. A. Kurg, K. Männik, L. Kousoulidou, C. Sismani, C. Pitta, D. Andreou, O. Zilina, S. Parkel, C. Tryphonos, C. Antoniadou, N. Tõnisson, P. Palta, T. Möls, M. Remm and P. C. Patsalis.
80/2:45 Novel Approaches to the Analysis and Detection of Chromosomal Abnormalities: 22q as a Model. B. S. Emanuel, J. A. S. Vorstman, G. R. Jalali, A. E. Urban, S. M. Weissman, M. Snyder and NimbleGen Inc.
81/3:00 Interstitial deletion of chromosome 9q22.32-q22.33: a novel cause of syndromic overgrowth. R. Redon, G. Baujat, D. Sanlaville, M. Le Merrer, M. Vekemans, N. Carter, A. Munnich, L. Colleaux and V. Cormier-Daire.
82/3:15 Cleidocranial Dysplasia Plus Vascular Anomalies With 6p21.2 Microdeletion Spanning RUNX2 and VEGF. K. Izumi, N. Yahagi, Y. Fujii, R. Kosaki, M. Higuchi, Y. Naito, G. Nishimura, T. Takahashi and K. Kosaki.
83/3:30 ZNF674: a novel XLMR gene identified through array CGH. A. P. M. de Brouwer, D. Lugtenberg, M. Banning, A. Oudakker, H. V. Firth, L. Willatt, J. Chelly, J. P. Fryns, H. H. Ropers, C. Moraine, H. G. Brunner, H. G. Yntema and H. van Bokhoven.
84/3:45 High-resolution analysis of genomic imbalance in children with mental retardation. J. M. Friedman, L. Arbour, L. Armstrong, D. Bailey, A. Baross, P. Birch, M. Brown-John, M. Cao, S. Chan, D. L. Charest, A. Delaney, P. Eydoux, N. Farnoud, N. Fernandes, S. Flibotte, W. Gibson, A. Go, R. Hanson, R. Holt and S. Jones.
85/4:00 Rapid prenatal diagnosis by microarray-based comparative genomic hybridization: Experience of a pilot program. T. Sahoo, A. Patel, P. Ward, S. Darilek, J. Li, D. del Gaudio, S. Kang, S. Lalani, I. Van den Veyver, S. McAdoo, A. Burke, B. Roa, C. Shaw, C. Chinault, S. Cheung, A. Beaudet and C. Eng.
86/4:15 An algorithm for cgh microarray in clinical practice. E. Aston, H. Whitby, T. Maxwell, B. Milash, B. Issa, J. Xu, Z. Chen and A. Brothman.
