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Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development. (2015)

First Author: Vivante A

Attributed to: Molecular bases of congenital bladder disease: the urofacial syndome (UFS) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.07.001

PubMed Identifier: 26235987

Publication URI: http://europepmc.org/abstract/MED/26235987

Type: Journal Article/Review

Volume: 97

Parent Publication: American journal of human genetics

Issue: 2

ISSN: 0002-9297