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    Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature
                                      
                                            Valli, Roberto,                              De Bernardi, Francesca,                              Frattini, Annalisa,                              Volpi, Luca,                              Bignami, Maurizio,                              Facchetti, Fabio,                              Pasquali, Francesco,                              Castelnuovo, Paolo,                              Maserati, Emanuela                              
Published in Genes chromosomes & cancer (01.12.2015)
                   
      
      
                                                  Published in Genes chromosomes & cancer (01.12.2015)
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          Molecular Karyotyping of Human Single Sperm by Array- Comparative Genomic Hybridization
                                      
                                            Patassini, Cristina,                              Garolla, Andrea,                              Bottacin, Alberto,                              Menegazzo, Massimo,                              Speltra, Elena,                              Foresta, Carlo,                              Ferlin, Alberto                              
Published in PloS one (02.04.2013)
                   
      
      
                                                  Published in PloS one (02.04.2013)
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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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          Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
                                      
                                            Osoegawa, K,                              Vessere, G M,                              Utami, K H,                              Mansilla, M A,                              Johnson, M K,                              Riley, B M,                              L’Heureux, J,                              Pfundt, R,                              Staaf, J,                              van der Vliet, W A,                              Lidral, A C,                              Schoenmakers, E F P M,                              Borg, A,                              Schutte, B C,                              Lammer, E J,                              Murray, J C,                              de Jong, P J                              
Published in Journal of medical genetics (01.02.2008)
                   
      
      
                                                  Published in Journal of medical genetics (01.02.2008)
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          Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization
                                      
                                            Moteki, Hideaki,                              Azaiez, Hela,                              Sloan-Heggen, Christina M,                              Booth, Kevin,                              Nishio, Shin-Ya,                              Wakui, Keiko,                              Yamaguchi, Tomomi,                              Kolbe, Diana L,                              Iwasa, Yoh-Ichiro,                              Shearer, A Eliot,                              Fukushima, Yoshimitsu,                              Smith, Richard J H,                              Usami, Shin-Ichi                              
Published in Annals of otology, rhinology & laryngology (01.11.2016)
                   
      
      
                                                  Published in Annals of otology, rhinology & laryngology (01.11.2016)
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          Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease
                                      
                                            Robak, Laurie A.,                              Du, Renqian,                              Yuan, Bo,                              Gu, Shen,                              Alfradique-Dunham, Isabel,                              Kondapalli, Vismaya,                              Hinojosa, Evelyn,                              Stillwell, Amanda,                              Young, Emily,                              Zhang, Chaofan,                              Song, Xiaofei,                              Du, Haowei,                              Gambin, Tomasz,                              Jhangiani, Shalini N.,                              Coban Akdemir, Zeynep,                              Muzny, Donna M.,                              Tejomurtula, Anusha,                              Ross, Owen A.,                              Shaw, Chad,                              Jankovic, Joseph,                              Bi, Weimin,                              Posey, Jennifer E.,                              Lupski, James R.,                              Shulman, Joshua M.                              
Published in Neurology. Genetics (01.10.2020)
                   
      
      
                                                  Published in Neurology. Genetics (01.10.2020)
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          Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization
                                      
                                            Fan, Yao-Shan,                              Jayakar, Parul,                              Zhu, Hongbo,                              Barbouth, Deborah,                              Sacharow, Stephanie,                              Morales, Ana,                              Carver, Virginia,                              Benke, Paul,                              Mundy, Peter,                              Elsas, Louis J                              
Published in Human mutation (01.11.2007)
                   
      
      
                                                  Published in Human mutation (01.11.2007)
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          High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization
                                      
                                            Zhang, Xiaoxiao,                              Snijders, Antoine,                              Segraves, Richard,                              Zhang, Xiuqing,                              Niebuhr, Anita,                              Albertson, Donna,                              Yang, Huanming,                              Gray, Joe,                              Niebuhr, Erik,                              Bolund, Lars,                              Pinkel, Dan                              
Published in American journal of human genetics (01.02.2005)
                   
      
      
                                                  Published in American journal of human genetics (01.02.2005)
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          Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
                                      
                                            Yu, Wei,                              Ballif, Blake C.,                              Kashork, Catherine D.,                              Heilstedt, Heidi A.,                              Howard, Leslie A.,                              Cai, Wei-Wen,                              White, Lisa D.,                              Liu, Wenbin,                              Beaudet, Arthur L.,                              Bejjani, Bassem A.,                              Shaw, Chad A.,                              Shaffer, Lisa G.                              
Published in Human molecular genetics (01.09.2003)
                   
      
      
                                                  Published in Human molecular genetics (01.09.2003)
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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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          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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          Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications
                                      
                                            Di Gregorio, Eleonora,                              Gai, Giorgia,                              Botta, Giovanni,                              Calcia, Alessandro,                              Pappi, Patrizia,                              Talarico, Flavia,                              Savin, Elisa,                              Ribotta, Marisa,                              Zonta, Andrea,                              Mancini, Cecilia,                              Giorgio, Elisa,                              Cavalieri, Simona,                              Restagno, Gabriella,                              Ferrero, Giovanni B.,                              Viora, Elsa,                              Pasini, Barbara,                              Grosso, Enrico,                              Brusco, Alfredo,                              Brussino, Alessandro                              
Published in Cytogenetic and genome research (01.01.2015)
                   
      
      
                                                  Published in Cytogenetic and genome research (01.01.2015)
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          Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements
                                      
                                            Sahoo, Trilochan,                              Shaw, Chad A.,                              Young, Andrew S.,                              Whitehouse, Nathan L.,                              Schroer, Richard J.,                              Stevenson, Roger E.,                              Beaudet, Arthur L.                              
Published in American journal of medical genetics. Part A (01.12.2005)
                   
      
      
                                                  Published in American journal of medical genetics. Part A (01.12.2005)
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          Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes
                                      
                                            Kawankar, Nikesh,                              Jijina, Farah,                              Ghosh, Kanjaksha,                              Vundinti, Babu Rao                              
Published in Cancer epidemiology (01.08.2011)
                   
      
      
                                                  Published in Cancer epidemiology (01.08.2011)
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          Aneuploidy screening by array comparative genomic hybridization improves success rates of in vitro fertilization: A multicenter Indian study
                                      
                                            Kotdawala, Aditi,                              Patel, Deven,                              Herrero, Javier,                              Khajuria, Rajni,                              Mahajan, Nalini,                              Banker, Manish                              
Published in Journal of human reproductive sciences (01.10.2016)
                   
      
      
                                                  Published in Journal of human reproductive sciences (01.10.2016)
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          Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
                                      
                                            Li, Yun Rose,                              Glessner, Joseph T.,                              Coe, Bradley P.,                              Li, Jin,                              Mohebnasab, Maede,                              Chang, Xiao,                              Connolly, John,                              Kao, Charlly,                              Wei, Zhi,                              Bradfield, Jonathan,                              Kim, Cecilia,                              Hou, Cuiping,                              Khan, Munir,                              Mentch, Frank,                              Qiu, Haijun,                              Bakay, Marina,                              Cardinale, Christopher,                              Lemma, Maria,                              Abrams, Debra,                              Bridglall-Jhingoor, Andrew,                              Behr, Meckenzie,                              Harrison, Shanell,                              Otieno, George,                              Thomas, Alexandria,                              Wang, Fengxiang,                              Chiavacci, Rosetta,                              Wu, Lawrence,                              Hadley, Dexter,                              Goldmuntz, Elizabeth,                              Elia, Josephine,                              Maris, John,                              Grundmeier, Robert,                              Devoto, Marcella,                              Keating, Brendan,                              March, Michael,                              Pellagrino, Renata,                              Grant, Struan F. A.,                              Sleiman, Patrick M. A.,                              Li, Mingyao,                              Eichler, Evan E.,                              Hakonarson, Hakon                              
Published in Nature communications (14.01.2020)
                   
      
      
                                                  Published in Nature communications (14.01.2020)
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          Characterization of hemizygous deletions in Citrus using array-Comparative Genomic Hybridization and microsynteny comparisons with the poplar genome
                                      
                                            Ríos, Gabino,                              Naranjo, Miguel A,                              Iglesias, Domingo J,                              Ruiz-Rivero, Omar,                              Geraud, Marion,                              Usach, Antonio,                              Talón, Manuel                              
Published in BMC genomics (09.08.2008)
                   
      
      
                                                  Published in BMC genomics (09.08.2008)
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