📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. (2019)

First Author: Van Der Sluijs PJ
Attributed to:  The Northern Ireland Genomic Medicine Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41436-018-0368-y

PubMed Identifier: 30696996

Publication URI: http://europepmc.org/abstract/MED/30696996

Type: Journal Article/Review

Volume: 21

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 9

ISSN: 1098-3600