Items where authors include "Leal, S"

Export as [feed] Atom [feed] RSS
Jump to: Article
Number of items: 2.

Article

Al-Jawahiri, R orcid.org/0000-0002-5689-3368, Foroutan, A, Kerkhof, J et al. (111 more authors) (2022) SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. Genetics in Medicine, 24 (6). pp. 1261-1273. ISSN 1098-3600

Sivakumar, S, Taccone, FS, Desai, KA et al. (2497 more authors) (2016) ESICM LIVES 2016: part two. Intensive Care Medicine Experimental, 4 (S1).

This list was generated on Sun Mar 24 04:24:00 2024 GMT.