Bruno Marino Taussig De Bodonia

Pubblicazioni

Titolo	Pubblicato in	Anno
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome	HUMAN GENETICS	2016
Congenital heart defects in Noonan syndrome and RIT1 mutation	GENETICS IN MEDICINE	2016
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2016
The embryology of the interatrial septum	Fetal and Hybrid Procedures in Congenital Heart Diseases	2016
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome	AMERICAN JOURNAL OF HUMAN GENETICS	2015
Left ventricular non compaction with aortic valve anomalies: A recurrent feature of 22q11.2 distal deletion syndrome	EUROPEAN JOURNAL OF MEDICAL GENETICS	2015
22q11.2 deletion syndrome	NATURE REVIEWS. DISEASE PRIMERS	2015
Hypoplastic left heart syndrome and 21q22.3 deletion	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2015
DETECTION OF CARDIOVASCULAR ABNORMALITIES IN PEDIATRIC PATIENTS WITH EHLERS-DANLOS SYNDROME: ROLE OF NEW ECHOCARDIOGRAPHIC TECHNIQUES	Giornale Italiano di CardiologiaGIORNALE ITALIANO DI CARDIOLOGIA	2015