Feingold Syndrome Type 1: a Rare Cause of Fetal Microcephaly (Prenatal Diagnosis)

AuthID
P-00Y-3QP
4
Author(s)
Gouveia, I
·
Godinho, C
·
Document Type
Article
Year published
2023
Published
in BMJ CASE REPORTS
Volume: 16, Issue: 3, Pages: e254366 (4)
Indexing
Publication Identifiers
Pubmed: 36889805
Scopus: 2-s2.0-85149621055
Wos: WOS:000957848300016
Export Publication Metadata
Marked List
Info
At this moment we don't have any links to full text documens.