DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Lozier ER, Konovalov FA, Kanivets IV. , et al.
De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features.
J Hum Genet 2018;
63 (08) 919-922
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