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Appropriateness of array‐CGH in the ADHD clinics: A comparative study
Baccarin, Marco, Picinelli, Chiara, Tomaiuolo, Pasquale, Castronovo, Paola, Costa, Anna, Verdecchia, Magda, Cannizzaro, Chiara, Barbieri, Giusi, Sacco, Roberto, Persico, Antonio M., Lintas, Carla
Published in Genes, brain and behavior (01.07.2020)
Published in Genes, brain and behavior (01.07.2020)
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Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects
Sagoo, Gurdeep S, Butterworth, Adam S, Sanderson, Simon, Shaw-Smith, Charles, Higgins, Julian P T, Burton, Hilary
Published in Genetics in medicine (01.03.2009)
Published in Genetics in medicine (01.03.2009)
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High Resolution X Chromosome-Specific Array-CGH Detects New CNVs in Infertile Males
Krausz, Csilla, Giachini, Claudia, Lo Giacco, Deborah, Daguin, Fabrice, Chianese, Chiara, Ars, Elisabet, Ruiz-Castane, Eduard, Forti, Gianni, Rossi, Elena
Published in PloS one (09.10.2012)
Published in PloS one (09.10.2012)
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High-Resolution Array CGH Analysis Identifies Regional Deletions and Amplifications of Chromosome 8 in Uveal Melanoma
Hammond, David W., Al-Shammari, Nawal S. D., Danson, Sarah, Jacques, Rhona, Rennie, Ian G., Sisley, Karen
Published in Investigative ophthalmology & visual science (01.06.2015)
Published in Investigative ophthalmology & visual science (01.06.2015)
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Copy number variants prioritization after array-CGH analysis – a cohort of 1000 patients
Carreira, Isabel Marques, Ferreira, Susana Isabel, Matoso, Eunice, Pires, Luís Miguel, Ferrão, José, Jardim, Ana, Mascarenhas, Alexandra, Pinto, Marta, Lavoura, Nuno, Pais, Cláudia, Paiva, Patrícia, Simões, Lúcia, Caramelo, Francisco, Ramos, Lina, Venâncio, Margarida, Ramos, Fabiana, Beleza, Ana, Sá, Joaquim, Saraiva, Jorge, de Melo, Joana Barbosa
Published in Molecular cytogenetics (30.12.2015)
Published in Molecular cytogenetics (30.12.2015)
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Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12
Cellamare, Angelo, Coccaro, Nicoletta, Nuzzi, Maria Cristina, Casieri, Paola, Tampoia, Marilina, Maggiolini, Flavia Angela Maria, Gentile, Mattia, Ficarella, Romina, Ponzi, Emanuela, Conserva, Maria Rosa, Cardarelli, Laura, Panarese, Annunziata, Antonacci, Francesca, Gesario, Antonia
Published in Genes (07.06.2021)
Published in Genes (07.06.2021)
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Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH
Tyson, C., Harvard, C., Locker, R., Friedman, J.M., Langlois, S., Lewis, M.E.S., Van Allen, M., Somerville, M., Arbour, L., Clarke, L., McGilivray, B., Yong, S.L., Siegel-Bartel, J., Rajcan-Separovic, E.
Published in American journal of medical genetics. Part A (15.12.2005)
Published in American journal of medical genetics. Part A (15.12.2005)
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Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics
Qiao, Y, Harvard, C, Tyson, C, Liu, X, Fawcett, C, Pavlidis, P, Holden, J. J. A, Lewis, M. E. S, Rajcan-Separovic, E
Published in Human genetics (01.08.2010)
Published in Human genetics (01.08.2010)
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15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH
Koochek, M, Harvard, C, Hildebrand, MJ, Van Allen, M, Wingert, H, Mickelson, E, Holden, JJA, Rajcan-Separovic, E, Lewis, MES
Published in Clinical genetics (01.02.2006)
Published in Clinical genetics (01.02.2006)
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Somatic mosaicism for copy number variation in differentiated human tissues
Piotrowski, Arkadiusz, Bruder, Carl E.G, Andersson, Robin, de Ståhl, Teresita Diaz, Menzel, Uwe, Sandgren, Johanna, Poplawski, Andrzej, von Tell, Desiree, Crasto, Chiquito, Bogdan, Adam, Bartoszewski, Rafal, Bebok, Zsuzsa, Krzyzanowski, Maciej, Jankowski, Zbigniew, Partridge, E. Christopher, Komorowski, Jan, Dumanski, Jan P
Published in Human mutation (01.09.2008)
Published in Human mutation (01.09.2008)
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BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1
Brunet, Anna, Armengol, Lluís, Heine, Damià, Rosell, Jordi, García-Aragonés, Manel, Gabau, Elisabeth, Estivill, Xavier, Guitart, Miriam
Published in BMC medical genetics (23.12.2009)
Published in BMC medical genetics (23.12.2009)
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A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH
Harvard, C, Malenfant, P, Koochek, M, Creighton, S, Mickelson, ECR, Holden, JJA, Lewis, MES, Rajcan-Separovic, E
Published in Clinical genetics (01.04.2005)
Published in Clinical genetics (01.04.2005)
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Array CGH Reveals Genomic Aberrations in Human Emphysema
Choi, Jin Soo, Lee, Woon Jeong, Baik, Seung Ho, Yoon, Hyoung Kyu, Lee, Kweon-Haeng, Kim, Yeul Hong, Lim, Young, Wang, Young-Pil
Published in Lung (01.06.2009)
Published in Lung (01.06.2009)
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Array CGH on human first polar bodies suggests that non-disjunction is not the predominant mechanism leading to aneuploidy
Gabriel, Alem S, Thornhill, Alan R, Gordon, Anthony, Brown, Anthony, Taylor, Jon, Bennett, Kate, Handyside, Alan H, Griffin, Darren K
Published in Journal of medical genetics (26.05.2011)
Published in Journal of medical genetics (26.05.2011)
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Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
Zhou, Bo, Ho, Steve S, Zhang, Xianglong, Pattni, Reenal, Haraksingh, Rajini R, Urban, Alexander E
Published in Journal of medical genetics (01.11.2018)
Published in Journal of medical genetics (01.11.2018)
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Limited tissue fixation times and whole genomic amplification do not impact array CGH profiles
Ghazani, A A, Arneson, N C R, Warren, K, Done, S J
Published in Journal of clinical pathology (01.03.2006)
Published in Journal of clinical pathology (01.03.2006)
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders
Ching, Michael S.L., Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S., Morrow, Eric M., Chen, Xiaoli, Mukaddes, Nahit M., Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E., Berry, Gerard T., Driscoll, Katherine, Engle, Elizabeth C., Friedman, Sandra, Gusella, James F., Hisama, Fuki M., Irons, Mira B., Lafiosca, Tina, LeClair, Elaine, Miller, David T., Neessen, Michael, Picker, Jonathan D., Rappaport, Leonard, Rooney, Cynthia M., Sarco, Dean P., Stoler, Joan M., Walsh, Christopher A., Wolff, Robert R., Zhang, Ting, Nasir, Ramzi H., Wu, Bai-Lin
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2010)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2010)
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Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility
Costantini, Alice, Skarp, Sini, Kämpe, Anders, Mäkitie, Riikka E., Pettersson, Maria, Männikkö, Minna, Jiao, Hong, Taylan, Fulya, Lindstrand, Anna, Mäkitie, Outi
Published in Frontiers in endocrinology (Lausanne) (10.07.2018)
Published in Frontiers in endocrinology (Lausanne) (10.07.2018)
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Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH
Tyson, Christine, Qiao, Ying, Harvard, Chansonette, Liu, Xudong, Bernier, Francois P, McGillivray, Barbara, Farrell, Sandra A, Arbour, Laura, Chudley, Albert E, Clarke, Lorne, Gibson, William, Dyack, Sarah, McLeod, Ross, Costa, Teresa, VanAllen, Margot I, Yong, Siu-li, Graham, Gail E, MacLeod, Patrick, Patel, Millan S, Hurlburt, Jane, Holden, Jeanette JA, Lewis, Suzanne ME, Rajcan-Separovic, Evica
Published in Molecular cytogenetics (11.11.2008)
Published in Molecular cytogenetics (11.11.2008)
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Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene
Serra, Gregorio, Felice, Sofia, Antona, Vincenzo, Di Pace, Maria Rita, Giuffrè, Mario, Piro, Ettore, Corsello, Giovanni
Published in Italian journal of pediatrics (04.05.2022)
Published in Italian journal of pediatrics (04.05.2022)
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