A Novel Homozygous Deletion in Ccdc32 Gene Causing Cardiofacioneurodevelopmental Syndrome: the Fourth Patient Reported

AuthID
 P-010-GC3
4
Author(s)
da Rocha, DF
·
Quental, R
·
Tipo de Documento
Article
Year published
2024
Publicado
in CLINICAL DYSMORPHOLOGY, ISSN: 0962-8827
Volume: 33, Número: 3, Páginas: 114-117 (4)
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Pubmed®
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Publication Identifiers
Pubmed: 38818818
SCOPUS: 2-s2.0-85194992548
Wos: WOS:001236196100005
Source Identifiers
ISSN: 0962-8827
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