Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome
Gestores bibliográficos
item.contributor.advisor
ORCID:
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
item.page.isbn
item.page.issn
item.page.issne
item.page.doiurl
item.page.extent
3
item.page.accessRights
item.page.other
item.page.references
Abstract
OBJECTIVE:
Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable c...
Description
Centro de Genética y Genómica
item.page.coverage.spatial
item.page.sponsorship
Citation
International Journal Pediatrics Otorhinolaryngology, 2012, 76(12):1726-8
item.page.dc.rights
item.page.dc.rights.url
Estadísticas de uso
2 1,5 1 0,5 0
Septiembre 2025Octubre 2025Noviembre 2025Diciembre 2025Enero 2026Febrero 2026Marzo 2026