De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. (2019)

First Author: Holt RJ
Attributed to:  Morphogenesis and growth of the eye in health and disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2019.07.005

PubMed Identifier: 31402090

Publication URI: http://europepmc.org/abstract/MED/31402090

Type: Journal Article/Review

Volume: 105

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297