المؤلفون: Calcagni G., Calvieri C., Baban A., Bianco F., Barracano R., Caputo M., Madrigali A., Kikina S. S., Perrone M. A., Digilio M. C., Pozzi M., Secinaro A., Sarubbi B., Galletti L., Gagliardi M. G., de Zorzi A., Drago F., Leonardi B.

المساهمون: Calcagni, G., Calvieri, C., Baban, A., Bianco, F., Barracano, R., Caputo, M., Madrigali, A., Kikina, S. S., Perrone, M. A., Digilio, M. C., Pozzi, M., Secinaro, A., Sarubbi, B., Galletti, L., Gagliardi, M. G., de Zorzi, A., Drago, F., Leonardi, B.

مصطلحات موضوعية: Cardiac magnetic resonance imaging (cMRI), Congenital heart disease (CHD), Genetic syndrome, Pulmonary valve replacement (PVR), Tetralogy of Fallot (ToF)

Relation: info:eu-repo/semantics/altIdentifier/pmid/35160301; info:eu-repo/semantics/altIdentifier/wos/WOS:000754824400001; volume:11; issue:3; firstpage:850; journal:JOURNAL OF CLINICAL MEDICINE; http://hdl.handle.net/11564/776787; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85123920818; https://www.mdpi.com/2077-0383/11/3/850

الاتاحة: http://hdl.handle.net/11564/776787
https://doi.org/10.3390/jcm11030850
https://www.mdpi.com/2077-0383/11/3/850