Candelo, E.
Caicedo, G.
Mejia, L.
Pachajoa, H.
Funding for this research was provided by:
Universidad Icesi
Centre for Research into Congenital Anomalies and Rare Diseases (CIACER)
This article is maintained by: Elsevier
Article Title: Chromosome 17p13.3 microdeletion syndrome with unaltered PAFAH1B1 gene
Journal Title: Neurología (English Edition)
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.nrleng.2018.10.003
CrossRef DOI link to the associated document: https://doi.org/10.1016/j.nrl.2016.10.001
Content Type: simple-article
Copyright: © 2018 Published by Elsevier España, S.L.U. on behalf of Sociedad Española de Neurología.