Array-Based Comparative Genomic Hybridization for the Detection of Copy Number Alterations in Single Cells
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-3621-3_11
Reference18 articles.
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2. Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T, Lichter P (1997) Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer 20(4):399–407
3. Fiorentino F (2012) Array comparative genomic hybridization: its role in preimplantation genetic diagnosis. Curr Opin Obstet Gynecol 24(4):203–209. https://doi.org/10.1097/GCO.0b013e328355854d
4. Munne S (2012) Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization. Curr Genomics 13(6):463–470. https://doi.org/10.2174/138920212802510457
5. Fiorentino F, Caiazzo F, Napolitano S, Spizzichino L, Bono S, Sessa M, Nuccitelli A, Biricik A, Gordon A, Rizzo G, Baldi M (2011) Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases. Prenat Diagn 31(13):1270–1282. https://doi.org/10.1002/pd.2884
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