Associated Papers
SETD1B variants associated with absence seizures.
Zhang G et al.
European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society, 2025
Genetic Characterization of Primary Mediastinal B-Cell Lymphoma: Pathogenesis and Patient Outcomes.
Noerenberg D et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology, 2024
38055913 (PubMed )
Supplement: DS3_JCO.23.01053.xlsx › Table_S2.7
Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome.
Weerts MJA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
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