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Expanding the phenotype of SETD5-related disorder and presenting a novel association with bone fragility. (2021)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cge.14014

PubMed Identifier: 34169511

Publication URI: http://europepmc.org/abstract/MED/34169511

Type: Journal Article/Review

Volume: 100

Parent Publication: Clinical genetics

Issue: 3

ISSN: 0009-9163