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An Amish founder variant consolidates disruption of CEP55 as a cause of hydranencephaly and renal dysplasia. (2019)

First Author: Rawlins LE

Attributed to: Precision Medicine Exeter Innovation Platform (PMEI Platform): Proof of Concept Funds funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-018-0306-0

PubMed Identifier: 30622327

Publication URI: http://europepmc.org/abstract/MED/30622327

Type: Journal Article/Review

Volume: 27

Parent Publication: European journal of human genetics : EJHG

Issue: 4

ISSN: 1018-4813