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Diagnosis and Management of Beckwith-Wiedemann Syndrome

Beckwith-Wiedemann syndrome (BWS) is a human genomic imprinting disorder that presents with a wide spectrum of clinical features including overgrowth, abdominal wall defects, macroglossia, neonatal hypoglycemia, and predisposition to embryonal tumors. It is associated with genetic and epigenetic cha...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Pediatr
Prif Awduron: Wang, Kathleen H., Kupa, Jonida, Duffy, Kelly A., Kalish, Jennifer M.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6990127/
https://ncbi.nlm.nih.gov/pubmed/32039119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2019.00562
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