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Familial severe skeletal Class II malocclusion with gingival hyperplasia caused by a complex structural rearrangement at the KCNJ2-KCNJ16 locus. (2024)

First Author: Maroofian R

Attributed to: Uncovering new mechanisms of craniosynostosis associated with structural and copy number variation, using mouse modelling and human neural crest cells funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.xhgg.2024.100352

PubMed Identifier: 39257002

Publication URI: http://europepmc.org/abstract/MED/39257002

Type: Journal Article/Review

Volume: 5

Parent Publication: HGG advances

Issue: 4

ISSN: 2666-2477