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

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:000480488500002Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysisResource Types::text::journal::journal article