Temple Syndrome By 14(Q32) Deletion Detected Prenatally By Array-Cgh

AuthID
 P-00Y-TX6
8
Author(s)
Ferreira, SI
·
Mascarenhas, A
·
Oliveira, D
·
de Melo, JB
Tipo de Documento
Abstract
Year published
2023
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 102, Número: 13
Conference
26Th Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 17-19, 2022, Location: Coimbra, PORTUGAL
Indexing
Wos®
Publication Identifiers
Wos: WOS:001005724900111
Source Identifiers
ISSN: 0025-7974
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