📣 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.

AI-based diagnosis and phenotype - Genotype correlations in syndromic craniosynostoses. (2024)

First Author: Hennocq Q

Attributed to: A hub for device personalisation in the treatment of congenital diseases funded by EPSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.jcms.2024.02.010

PubMed Identifier: 39187417

Publication URI: http://europepmc.org/abstract/MED/39187417

Type: Journal Article/Review

Volume: 52

Parent Publication: Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery

Issue: 10

ISSN: 1010-5182