Publication | Open Access
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
86
Citations
27
References
2016
Year
Allelic VariantSystems BiologySomatic VariantGenetic DisorderGeneticsRecognizable Clinical PhenotypeMolecular GeneticsGene ExpressionMedicineAsxl2 Are AssociatedVariant Interpretation
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