A Familial Case with a Zmynd11 Mutation: Syndromic Intellectual Disability with a Recognizable Phenotype

AuthID
 P-00Q-ZEW
3
Author(s)
Tipo de Documento
Abstract
Year published
2019
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 98, Número: 26
Conference
22Nd Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 15-17, 2018, Location: Porto, PORTUGAL, Patrocinadores: Portuguese Soc Human Genet
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Wos®
Publication Identifiers
Wos: WOS:000480733400153
Source Identifiers
ISSN: 0025-7974
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