Two Prenatal Cases with a Variant of Loss in Homozygosity Involving the Crppa (Ispd) Gene

AuthID
 P-00W-HMP
8
Author(s)
Ventura, C
·
Lemos, R
·
Costa, P
·
Teixeira, M
·
Sa, J
·
Soares, G
·
Cerqueira, R
Tipo de Documento
Abstract
Year published
2022
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 30, Número: SUPPL 1, Páginas: 93-93 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000779367700234
Source Identifiers
ISSN: 1018-4813
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