v1
ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation.
Identifier:nobleid.org/w1/20260515/64EE9B06
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/64EE9B06)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →