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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. (2021)

First Author: Den Hoed J

Attributed to: Developing diagnostic methods for clinical genetics - phenotyping from faces in photos. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.01.007

PubMed Identifier: 33513338

Publication URI: http://europepmc.org/abstract/MED/33513338

Type: Journal Article/Review

Volume: 108

Parent Publication: American journal of human genetics

Issue: 2

ISSN: 0002-9297