Report Of A Rare 18P11.32P11.21 Terminal Deletion In A Fetus With Multiple Anomalies

AuthID
 P-00Y-TVF
15
Author(s)
Serafim, SS
·
Pedro, SI
·
Brito, FT
·
Tarelho, AR
·
Peliano, RC
·
Cohen, AE
·
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:001005724900113
Source Identifiers
ISSN: 0025-7974
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