Erger, F., Burau, K., Elsässer, M., Zimmermann, K., Moog, U., & Netzer, C. (2018). Uniparental isodisomy as a cause of recessive Mendelian disease: A diagnostic pitfall with a quick and easy solution in medium/large NGS analyses. European journal of human genetics, 26(9), . https://doi.org/10.1038/s41431-018-0195-2
Chicago-Zitierstil (17. Ausg.)Erger, Florian, Karin Burau, Michael Elsässer, Katharina Zimmermann, Ute Moog, und Christian Netzer. "Uniparental Isodisomy as a Cause of Recessive Mendelian Disease: A Diagnostic Pitfall with a Quick and Easy Solution in Medium/large NGS Analyses." European Journal of Human Genetics 26, no. 9 (2018). https://doi.org/10.1038/s41431-018-0195-2.
MLA-Zitierstil (9. Ausg.)Erger, Florian, et al. "Uniparental Isodisomy as a Cause of Recessive Mendelian Disease: A Diagnostic Pitfall with a Quick and Easy Solution in Medium/large NGS Analyses." European Journal of Human Genetics, vol. 26, no. 9, 2018, https://doi.org/10.1038/s41431-018-0195-2.