Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis

Journal

Orphanet Journal of Rare Diseases

ISSN

1750-1172

Date Issued

2019

Author(s)

M. Fernanda Rozas

BENAVIDES GONZALEZ, FELIPE ORLANDO

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

Luis León

REPETTO LISBOA, MARIA GABRIELA

Facultad de Medicina Clínica Alemana Universidad del Desarrollo

Type

Resource Types::text::journal::journal article

DOI

10.1186/s13023-019-1170-x

URL

https://investigadores.udd.cl/handle/123456789/3625

Project(s)

Genetic modifiers of the cardiovascular phenotype of chromosome 22q11 micro deletion syndrome: Next-generation sequencing of candidate regions identified by genome-wide association analysis

Prodromal manifestations of Parkinson´s disease in a high-risk population: 22q11.2 microdeletion syndrome

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