Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndromeGenomic and Functional Overlap between Somatic and Germline Chromosomal RearrangementsGenomic and transcriptomic plasticity in treatment-naive ovarian cancerVariants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndromeA de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorderGermline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle controlMate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations
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Karen Duran