Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2). (2013)

First Author: Khonsari RH

Attributed to: MRC Centre for Transplantation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddt041

PubMed Identifier: 23390131

Publication URI: http://europepmc.org/abstract/MED/23390131

Type: Journal Article/Review

Volume: 22

Parent Publication: Human molecular genetics

Issue: 9

ISSN: 0964-6906