Multiple postnatal craniofacial anomalies are characterized by conditional loss of polycystic kidney disease 2 (Pkd2) (2013)
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
Parent Publication: Human Molecular Genetics
Issue: 9
ISSN: 0964-6906