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European Journal of Medical Genetics|December 29, 2012
Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosisM Cristina Digilio, Laura Bernardini, Federica Consoli, et al.American Journal of Medical Genetics. Part A|November 16, 2019
Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosisAnwar Baban, Rachele Adorisio, Bernadette Corica, et al.Biomolecules|November 27, 2024
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic DiagnosticsMaria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, et al.International Journal of Cardiology|July 26, 2018
Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experienceAnwar Baban, Nicoletta Cantarutti, Rachele Adorisio, et al.Journal of Cardiovascular Development and Disease|October 26, 2022
Cardiovascular Involvement in Pediatric FLNC Variants: A Case Series of Fourteen PatientsAnwar Baban, Viola Alesi, Monia Magliozzi, et al.BMC Medical Genetics|January 24, 2014
Diagnosis of Noonan syndrome and related disorders using target next generation sequencingFrancesca Romana Lepri, Rossana Scavelli, Maria Cristina Digilio, et al.Journal of Cardiovascular Development and Disease|February 24, 2022
Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?Valentina Lodato, Giovanni Parlapiano, Federica Calì, et al.Italian Journal of Pediatrics|August 25, 2024
Biallelic NEXN variants and fetal onset dilated cardiomyopathy: two independent case reports and revision of literatureIrene Picciolli, Angelo Ratti, Berardo Rinaldi, et al.American Journal of Medical Genetics. Part A|April 23, 2020
Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defectAnwar Baban, Nicole Olivini, Nicoletta Cantarutti, et al.American Journal of Medical Genetics. Part A|September 30, 2014
Identification of TBX5 mutations in a series of 94 patients with Tetralogy of FallotAnwar Baban, Alex Vincent Postma, Monica Marini, et al.Pageof 10