受强制性开放获取政策约束的文章 - Aleksandar Petlichkovski了解详情
可在其他位置公开访问的文章：2 篇
Expanding the clinical phenotype of the ultra‐rare Skraban‐Deardorff syndrome: Two novel individuals with WDR26 loss‐of‐function variants and a literature review
L Pavinato, S Trajkova, E Grosso, E Giorgio, A Bruselles, FC Radio, ...
American Journal of Medical Genetics Part A 185 (6), 1712-1720, 2021
强制性开放获取政策： US National Institutes of Health, Government of Italy
DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity
S Trajkova, J Kerkhof, MR Sebastiano, L Pavinato, E Ferrero, C Giovenino, ...
Human Genetics and Genomics Advances 5 (3), 2024
强制性开放获取政策： National Institute for Health Research, UK
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