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by Gutin, Alexander and Vecchietti, Alberto and Chen, Zhoutao and Sterck, Lieven and Gardiner, Susan E and Cestaro, Alessandro and Niazi, Faheem and Bus, Vincent and Rouzé, Pierre and Lespinasse, Yves and Chagné, David and Komjanc, Matteo and Micheletti, Diego and Kodira, Chinnappa and Bhatnagar, Satish K and Ederle, Davide and Tao, Quanzhou and Stormo, Aimee and Gleave, Andrew P and Dal Ri, Antonio and Skolnick, Mark and Cavaiuolo, Marina and Palmer, Melinda and Fontana, Paolo and Eldredge, Glenn and Dhingra, Amit and Kalyanaraman, Ananth and Si-Ammour, Azeddine and Masiero, Simona and Costa, Fabrizio and Lavezzo, Enrico and Egholm, Michael and Macalma, Teresita and Fawcett, Jeffrey A and Fitzgerald, Lisa M and Lazzari, Barbara and Jiwan, Derick and Bogden, Robert and Wu, Changjun and Cova, Valentina and Castelletti, Sara and Gutin, Natalia and Wardell, Bryan and Viola, Roberto and Chu, Vu T and Mitchell, Jeff T and Vick, Jessica and Crowhurst, Ross N and Goremykin, Vadim and Toppo, Stefano and Salamini, Francesco and Malacarne, Giulia and Troggio, Michela and Desany, Brian and Coppola, Giuseppina and Pruss, Dmitry and Baldi, Paolo and Vezzulli, Silvia and Bumgarner, Roger E and King, Stephen T and Kater, Martin M and Allan, Andrew C and Durel, Charles-Eric and Stella, Alessandra and Lasserre, Pauline and Van de Peer, Yves and Affourtit, Jason and Malnoy, Mickael and Proost, Sebastian and Velasco, Riccardo and Perazzolli, Michele and Hellens, Roger P and Schaeffer, Scott and Salvi, Silvio and Krishnan, Vandhana and Magnago, Pierluigi and Zharkikh, Andrey and Mraz, Amy and Longhi, Sara and Lanchbury, Jerry and Zini, Elena and Stormo, Keith and Koepke, Tyson and Moretto, Marco and Reid, Julia and Pindo, Massimo
Nature Genetics, ISSN 1061-4036, 10/2010, Volume 42, Issue 10, pp. 833 - 839
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2007, Volume 2, Issue 12, p. e1326
Journal Article
Journal Article
Journal of Experimental and Clinical Cancer Research, ISSN 1756-9966, 2014, Volume 33, Issue 1, pp. 74 - 74
Background: Conventional Sanger sequencing reliably detects the majority of genetic mutations associated with hereditary cancers, such as single-base changes... 
Large genomic rearrangements | Hereditary breast and ovarian cancer | Genetic screening | Lynch syndrome | Microarray analysis | NONPOLYPOSIS COLORECTAL-CANCER | HYBRIDIZATION | BRCA1 | MLH1 | BREAST | MSH2 | GENE | ONCOLOGY | FAMILIES | DELETIONS | Genetic research | Diagnosis | Instrument industry | Genes | Cancer
Journal Article
Diabetes care, ISSN 0149-5992, 02/2019, Volume 42, Issue 2, pp. 192 - 199
Journal Article
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