M. Fernanda RozasBENAVIDES GONZALEZ, FELIPE ORLANDOFELIPE ORLANDOBENAVIDES GONZALEZLuis LeónREPETTO LISBOA, MARIA GABRIELAMARIA GABRIELAREPETTO LISBOA2022-10-032022-10-032019Rozas, M. F., Benavides, F., León, L., & Repetto, G. M. (2019). Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: Systematic review and meta-analysis. Orphanet Journal of Rare Diseases, 14(1), 195. https://doi.org/10.1186/s13023-019-1170-xhttp://hdl.handle.net/11447/2983https://investigadores.udd.cl/handle/123456789/362510.1186/s13023-019-1170-x2-s2.0-85070475677WOS:000480488500002congenital heart defectschromosome 22q112 deletion syndromedigeorge syndromemeta-analysispalate anomaliessystematic reviewvelocardiofacial syndromearachnodactylychromosome deletioncraniosynostoseshumansmarfan syndromephenotypeaortic arch interruptionarticlechileanchromosome deletion 22q11cleft lip palatecleft palatecongenital heart diseasedisease coursefallot tetralogygene deletiongenetic associationheart atrium septum defectheart right ventricle double outletheart ventricle septum defecthumanpalate malformationpalatopharyngeal incompetencephenotypepulmonary valve atresiasegmental duplicationsystematic reviewarachnodactylychromosome deletioncraniofacial synostosisgeneticsmarfan syndromemeta analysisphenotypeAssociation between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysisResource Types::text::journal::journal article