Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes

The frequency of disease-related large rearrangements (referred to as copy-number mutations, CNMs) varies among genes, and search for these mutations has an important place in diagnostic strategies. In recent years, CGH method using custom-designed high-density oligonucleotide-based arrays allowed t...

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Huvudupphovsmän: Vasson, Aurélie, Leroux, Céline, Orhant, Lucie, Boimard, Mathieu, Toussaint, Aurélie, Leroy, Chrystel, Commere, Virginie, Ghiotti, Tiffany, Deburgrave, Nathalie, Saillour, Yoann, Atlan, Isabelle, Fouveaut, Corinne, Beldjord, Cherif, Valleix, Sophie, Leturcq, France, Dodé, Catherine, Bienvenu, Thierry, Chelly, Jamel, Cossée, Mireille
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2013
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3746255/
https://ncbi.nlm.nih.gov/pubmed/23340513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.279
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