An algorithm to identify patients aged 0–3 with rare genetic disorders.

Autor: Webb, Bryn D.^1,2 (AUTHOR) bdwebb@wisc.edu, Lau, Lisa Y.² (AUTHOR), Tsevdos, Despina³ (AUTHOR), Shewcraft, Ryan A.² (AUTHOR), Corrigan, David² (AUTHOR), Shi, Lisong² (AUTHOR), Lee, Seungwoo² (AUTHOR), Tyler, Jonathan² (AUTHOR), Li, Shilong² (AUTHOR), Wang, Zichen² (AUTHOR), Stolovitzky, Gustavo² (AUTHOR), Edelmann, Lisa² (AUTHOR), Chen, Rong² (AUTHOR), Schadt, Eric E.⁴ (AUTHOR), Li, Li² (AUTHOR) dlleely@gmail.com

Publikováno v: Orphanet Journal of Rare Diseases. 5/2/2024, Vol. 19 Issue 1, p1-8. 8p.