Items where authors include "Yonezawa, Y"

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Al-Jawahiri, R, 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

This list was generated on Mon Apr 15 02:22:07 2024 BST.