Autor: Céline Jost
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Tyrosine kinase inhibitors in Kosaki/Penttinen syndromes: new reports, follow-up of treated individuals and literature review
European Journal of Human Genetics, Published online: 08 July 2026; doi:10.1038/s41431-026-02153-3Tyrosine kinase inhibitors in Kosaki/Penttinen syndromes: new reports, follow-up of treated individuals and literature review
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De novo heterozygous variants of the <i>RSF1</i> gene are responsible for a syndromic neurodevelopmental disorder
European Journal of Human Genetics, Published online: 28 January 2026; doi:10.1038/s41431-026-02017-wDe novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder