A Rare Case of Fetal Skeletal Dysplasia: Tar Syndrome

AuthID
P-00W-HJ5
6
Author(s)
Perez, S
·
Carrilho, B
·
Bernardo, A
·
Cohen, A
·
Carvalho, I
Document Type
Abstract
Year published
2022
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 30, Issue: SUPPL 1, Pages: 113-113 (1)
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Publication Identifiers
Wos: WOS:000779367700291
Source Identifiers
ISSN: 1018-4813
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