Application of full-genome analysis to diagnose rare monogenic disorders.
Autor: | Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario |
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Zdroj: | NPJ Genomic Medicine; 10/13/2021, Vol. 6 Issue 1, p1-10, 10p |
Databáze: | Complementary Index |
Externí odkaz: |