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De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. (2017)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3765

PubMed Identifier: 28067911

Publication URI: http://europepmc.org/abstract/MED/28067911

Type: Journal Article/Review

Volume: 49

Parent Publication: Nature genetics

Issue: 2

ISSN: 1061-4036