Merritt, David (1999). "Black holes and galaxy evolution". In Combes, F.; Mamon, G. A.; Charmandaris, V. (eds.). Dynamics of Galaxies: From the Early Universe to the Present. Publications of the Astronomical Society of the Pacific. Vol. 197. pp. 221–232. arXiv:astro-ph/9910546. Bibcode:2000ASPC..197..221M. ISBN 978-1-58381-024-8. 978-1-58381-024-8
Cummings, Sue (1999-09-22). "The Flux in Pop Music Has a Distinctly Download Beat to It". The New York Times. Retrieved 2013-11-01. https://www.nytimes.com/1999/09/22/business/the-flux-in-pop-music-has-a-distinctly-download-beat-to-it.html
DiNucci, Darcy (1999). "Fragmented Future" (PDF). Print. 53 (4): 32. Archived (PDF) from the original on 2011-11-10. Retrieved 2011-11-04. http://darcyd.com/fragmented_future.pdf
Crilly, Tony (2007). 50 Mathematical Ideas you really need to know. London: Quercus. p. 117. ISBN 978-1-84724-008-8. 978-1-84724-008-8
Hales, Thomas C. (January 2001). "The Honeycomb Conjecture". Discrete and Computational Geometry. 25 (1): 1–22. arXiv:math/9906042. doi:10.1007/s004540010071. MR 1797293. S2CID 14849112. /wiki/Discrete_and_Computational_Geometry
Randall, Lisa; Sundrum, Raman (1999). "Large Mass Hierarchy from a Small Extra Dimension". Physical Review Letters. 83 (17): 3370–3. arXiv:hep-ph/9905221. Bibcode:1999PhRvL..83.3370R. doi:10.1103/PhysRevLett.83.3370. /wiki/Physical_Review_Letters
Randall, Lisa; Sundrum, Raman (1999). "An Alternative to Compactification". Physical Review Letters. 83 (23): 4690–3. arXiv:hep-th/9906064. Bibcode:1999PhRvL..83.4690R. doi:10.1103/PhysRevLett.83.4690. S2CID 18530420. /wiki/ArXiv_(identifier)
Lucas, R. J.; Freedman, M. S.; Muñoz, M.; Garcia-Fernández, J. M.; Foster, R. G. (1999-04-16). "Regulation of the mammalian pineal by non-rod, non-cone, ocular photoreceptors". Science. 284 (5413): 505–507. Bibcode:1999Sci...284..505L. doi:10.1126/science.284.5413.505. ISSN 0036-8075. PMID 10205062. https://www.science.org/doi/10.1126/science.284.5413.505
Amir, Ruthie E.; Van den Veyver, Ignatia; Wan, Mimi; Tran, Charles; Francke, Uta; Zoghbi, Huda Y. (1999). "Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2". Nature Genetics. 23 (2): 185–8. doi:10.1038/13810. PMID 10508514. S2CID 3350350. https://www.nature.com/articles/ng1099_185