Publication | Closed Access
De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features
37
Citations
8
References
2018
Year
Genetic DisorderGeneticsFragile X SpectrumPathologyDisease Gene IdentificationNonsense MutationDysmorphic FeaturesMedicineVariant InterpretationDevelopmental Delay
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