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Bruno Marino

Showing results (51-60 of 156) with videos related to

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American Journal of Medical Genetics. Part A|January 12, 2005
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresiaAnna Sarkozy, Emanuela Conti, Rita D'Agostino, et al.
The American Journal of Cardiology|March 23, 2011
Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndromeGiancarlo Tancredi, Paolo Versacci, Anna Maria Pasquino, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 25, 2009
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defectsGuido Michielon, Bruno Marino, Gianluca Oricchio, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
LEOPARD syndrome: clinical diagnosis in the first year of lifeM Cristina Digilio, Anna Sarkozy, Andrea de Zorzi, et al.
American Journal of Medical Genetics. Part A|July 28, 2025
Variable Intrafamilial Cardiac Phenotype Segregating With a TBX20 Missense Variant in the Putative Transcriptional Activation DomainGioia Mastromoro, Alice Traversa, Daniele Guadagnolo, et al.
Clinical Dysmorphology|March 15, 2006
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of FallotPasquale Vergara, Maria Cristina Digilio, Andrea De Zorzi, et al.
American Journal of Medical Genetics. Part A|January 26, 2005
Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2M Cristina Digilio, Bruno Marino, Rossella Capolino, et al.
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 18, 2008
Folic acid and methionine in the prevention of teratogen-induced congenital defects in miceDaria Cipollone, Rita Carsetti, Angela Tagliani, et al.
Pageof 16

Showing results (51-60 of 156) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Part A|January 12, 2005
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresiaAnna Sarkozy, Emanuela Conti, Rita D'Agostino, et al.
The American Journal of Cardiology|March 23, 2011
Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndromeGiancarlo Tancredi, Paolo Versacci, Anna Maria Pasquino, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 25, 2009
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defectsGuido Michielon, Bruno Marino, Gianluca Oricchio, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
LEOPARD syndrome: clinical diagnosis in the first year of lifeM Cristina Digilio, Anna Sarkozy, Andrea de Zorzi, et al.
American Journal of Medical Genetics. Part A|July 28, 2025
Variable Intrafamilial Cardiac Phenotype Segregating With a TBX20 Missense Variant in the Putative Transcriptional Activation DomainGioia Mastromoro, Alice Traversa, Daniele Guadagnolo, et al.
Clinical Dysmorphology|March 15, 2006
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of FallotPasquale Vergara, Maria Cristina Digilio, Andrea De Zorzi, et al.
American Journal of Medical Genetics. Part A|January 26, 2005
Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2M Cristina Digilio, Bruno Marino, Rossella Capolino, et al.
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 18, 2008
Folic acid and methionine in the prevention of teratogen-induced congenital defects in miceDaria Cipollone, Rita Carsetti, Angela Tagliani, et al.
Pageof 16