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M C Digilio

Showing results (51-60 of 130) with videos related to

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American Journal of Medical Genetics|November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotypeA Giannotti, M C Digilio, B Marino, et al.
Pediatric Cardiology|October 1, 1991
Turner's syndrome with atrioventricular canalB Marino, M C Digilio, M Papa, et al.
The Journal of Pediatrics|April 1, 1997
Conotruncal heart defects and chromosome 22q11 microdeletionM C Digilio, B Marino, A Giannotti, et al.
Minerva Pediatrica|January 1, 1992
[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case]A Giannotti, A Alessandri, A Reale, et al.
European Journal of Pediatrics|July 1, 1993
Discrete membranous subaortic stenosis in siblingsM C Digilio, A Giannotti, B Marino, et al.
Pediatric Cardiology|July 1, 1996
Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndromeB Marino, M C Digilio, M G Gagliardi, et al.
American Journal of Medical Genetics|September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18pM C Digilio, B Marino, A Giannotti, et al.
Teratology|April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canalM C Digilio, B Marino, A M Musolino, et al.
The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.
Pediatric Cardiology|March 15, 2002
Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndromeU Giordano, A Turchetta, A Giannotti, et al.
Pageof 13

Showing results (51-60 of 130) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|November 15, 1994
Cayler cardiofacial syndrome and del 22q11: part of the CATCH22 phenotypeA Giannotti, M C Digilio, B Marino, et al.
Pediatric Cardiology|October 1, 1991
Turner's syndrome with atrioventricular canalB Marino, M C Digilio, M Papa, et al.
The Journal of Pediatrics|April 1, 1997
Conotruncal heart defects and chromosome 22q11 microdeletionM C Digilio, B Marino, A Giannotti, et al.
Minerva Pediatrica|January 1, 1992
[Partial deletion of the long arm of chromosome 17. Presentation of a clinical case]A Giannotti, A Alessandri, A Reale, et al.
European Journal of Pediatrics|July 1, 1993
Discrete membranous subaortic stenosis in siblingsM C Digilio, A Giannotti, B Marino, et al.
Pediatric Cardiology|July 1, 1996
Partial atrioventricular canal with left-sided obstruction in patients with Noonan syndromeB Marino, M C Digilio, M G Gagliardi, et al.
American Journal of Medical Genetics|September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18pM C Digilio, B Marino, A Giannotti, et al.
Teratology|April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canalM C Digilio, B Marino, A M Musolino, et al.
The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.
Pediatric Cardiology|March 15, 2002
Exercise testing and 24-hour ambulatory blood pressure monitoring in children with Williams syndromeU Giordano, A Turchetta, A Giannotti, et al.
Pageof 13