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Orphanet Journal of Rare Diseases
|
October 6, 2010
Acro-cardio-facial syndrome
Maria Cristina Digilio, Bruno Dallapiccola
Frontiers in Pediatrics
|
December 20, 2016
What Is New in Genetics of Congenital Heart Defects?
Maria Cristina Digilio, Bruno Marino
Current Opinion in Pediatrics
|
July 20, 2018
Cardiovascular disease in Noonan syndrome
Mary Ella Pierpont, Maria Cristina Digilio
Orphanet Journal of Rare Diseases
|
May 29, 2008
Leopard syndrome
Anna Sarkozy, Maria Cristina Digilio, Bruno Dallapiccola
The Journal of Thoracic and Cardiovascular Surgery
|
August 29, 2007
Familial recurrence of discrete membranous subaortic stenosis
Gerardo Piacentini, Bruno Marino, Maria Cristina Digilio
The Annals of Thoracic Surgery
|
June 26, 2003
Tetralogy of Fallot with aortic valvular stenosis and deletion 22q11
Bruno Marino, Federica Mileto, Maria Cristina Digilio
American Journal of Medical Genetics. Part A
|
February 22, 2005
Association of deletion 22 and trisomy 21: a likely random association in patients with conotruncal heart defects
Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Cardiology in the Young
|
March 24, 2006
Types of cardiac defects in children with Down's syndrome
Silvia Placidi, Maria Cristina Digilio, Bruno Marino
The Annals of Thoracic Surgery
|
November 27, 2007
GATA4 as candidate gene for pericardial defects
Claudia Saffirio, Bruno Marino, Maria Cristina Digilio
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2006
Atrioventricular canal defect in Bardet-Biedl syndrome: clinical evidence supporting the link between atrioventricular canal defect and polydactyly syndromes with ciliary dysfunction536
Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Page
of 24
Search research articles
Search
Showing results (1-10 of 232) with videos related to
Sort By:
Page
of 24
Orphanet Journal of Rare Diseases
|
October 6, 2010
Acro-cardio-facial syndrome
Maria Cristina Digilio, Bruno Dallapiccola
Frontiers in Pediatrics
|
December 20, 2016
What Is New in Genetics of Congenital Heart Defects?
Maria Cristina Digilio, Bruno Marino
Current Opinion in Pediatrics
|
July 20, 2018
Cardiovascular disease in Noonan syndrome
Mary Ella Pierpont, Maria Cristina Digilio
Orphanet Journal of Rare Diseases
|
May 29, 2008
Leopard syndrome
Anna Sarkozy, Maria Cristina Digilio, Bruno Dallapiccola
The Journal of Thoracic and Cardiovascular Surgery
|
August 29, 2007
Familial recurrence of discrete membranous subaortic stenosis
Gerardo Piacentini, Bruno Marino, Maria Cristina Digilio
The Annals of Thoracic Surgery
|
June 26, 2003
Tetralogy of Fallot with aortic valvular stenosis and deletion 22q11
Bruno Marino, Federica Mileto, Maria Cristina Digilio
American Journal of Medical Genetics. Part A
|
February 22, 2005
Association of deletion 22 and trisomy 21: a likely random association in patients with conotruncal heart defects
Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Cardiology in the Young
|
March 24, 2006
Types of cardiac defects in children with Down's syndrome
Silvia Placidi, Maria Cristina Digilio, Bruno Marino
The Annals of Thoracic Surgery
|
November 27, 2007
GATA4 as candidate gene for pericardial defects
Claudia Saffirio, Bruno Marino, Maria Cristina Digilio
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2006
Atrioventricular canal defect in Bardet-Biedl syndrome: clinical evidence supporting the link between atrioventricular canal defect and polydactyly syndromes with ciliary dysfunction536
Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Page
of 24