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

Published 2019 View Full Article

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Title
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 105, Issue 3, Pages 640-657
Publisher
Elsevier BV
Online
2019-08-08
DOI
10.1016/j.ajhg.2019.07.005

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