Lin, B.M., Grinde, K.E., Köttgen, A. und Franceschini, N. (2021) Whole genome sequence analyses of e GFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium [cd]. Freiburg: Universität. doi:10.1016/j.ebiom.2020.103157.
Chicago Manual of Style 17th edition (full note)Lin, Bridget M, Kelsey E Grinde, Anna Köttgen, und Nora Franceschini. Whole genome sequence analyses of e GFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. Cd. Freiburg: Universität, [2021?], Freiburg: Universität, [2021?]. https://doi.org/10.1016/j.ebiom.2020.103157.
American Psychological Association 7th editionLin, B. M., Grinde, K. E., Köttgen, A., & Franceschini, N. (ca. 2021). Whole genome sequence analyses of e GFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium [Cd]. Universität. https://doi.org/10.1016/j.ebiom.2020.103157
Modern Language Association 9th editionLin, B. M., K. E. Grinde, A. Köttgen, und N. Franceschini. Whole genome sequence analyses of e GFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. cd, Universität, 2021, https://doi.org/10.1016/j.ebiom.2020.103157.
ISO-690 (author-date, Deutsch)LIN, Bridget M, Kelsey E GRINDE, Anna KÖTTGEN und Nora FRANCESCHINI, 2021. Whole genome sequence analyses of e GFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. Freiburg: Universität