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Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants. (2017)

First Author: Savastano CP

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cge.12823

PubMed Identifier: 27350171

Publication URI: http://europepmc.org/abstract/MED/27350171

Type: Journal Article/Review

Volume: 91

Parent Publication: Clinical genetics

Issue: 5

ISSN: 0009-9163