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

AuthID
 P-00Y-3QP
4
Author(s)
Gouveia, I
·
Godinho, C
·
Castedo, S
Document Type
Article
Year published
2023
Published
in BMJ CASE REPORTS
Volume: 16, Issue: 3
Indexing
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Publication Identifiers
Pubmed: 36889805
Scopus: 2-s2.0-85149621055
Wos: WOS:000957848300016
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