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Co-occurrence of a maternally inherited DNMT3A duplication and a paternally inherited pathogenic variant in EZH2 in a child with growth retardation and severe short stature: atypical Weaver syndrome or evidence of a DNMT3A dosage effect?

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Description scientific article published on 01 August 2018
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author: Katarzyna Polonis 

Publication date August 1, 2018
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