Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting
| Autor: | Villela, Darine, Costa, Silvia Souza, Vianna-Morgante, Angela M., Krepischi, Ana C.V., Rosenberg, Carla |
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| Zdroj: | In European Journal of Medical Genetics December 2017 60(12):667-674 |
| Databáze: | ScienceDirect |
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