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M C Digilio

Showing results (71-80 of 130) with videos related to

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Journal of Medical Genetics|December 10, 1997
Radial aplasia and chromosome 22q11 deletionM C Digilio, A Giannotti, B Marino, et al.
American Journal of Medical Genetics|June 22, 1999
Genetic heterogeneity of isolated noncompaction of the left ventricular myocardiumM C Digilio, B Marino, M Bevilacqua, et al.
American Journal of Diseases of Children (1960)|December 1, 1993
Risk of congenital heart defects in relatives of patients with atrioventricular canalM C Digilio, B Marino, M P Cicini, et al.
The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.
American Journal of Medical Genetics|November 7, 1998
Noonan syndrome and aortic coarctationM C Digilio, B Marino, F Picchio, et al.
Minerva Pediatrica|June 1, 1991
[The life style and physical activity of the child operated on for congenital cardiopathy]F Drago, M C Digilio, S Giannico, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Cytogenetic and Genome Research|August 17, 2005
Pure trisomy 19p syndrome in an infant with an extra ring chromosomeA Novelli, C Ceccarini, L Bernardini, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 13, 2000
Antigliadin and antiendomysial antibodies in children with Down's syndromeB Papadatou, F Ferretti, A Giannotti, et al.
Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, et al.
Pageof 13

Showing results (71-80 of 130) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|December 10, 1997
Radial aplasia and chromosome 22q11 deletionM C Digilio, A Giannotti, B Marino, et al.
American Journal of Medical Genetics|June 22, 1999
Genetic heterogeneity of isolated noncompaction of the left ventricular myocardiumM C Digilio, B Marino, M Bevilacqua, et al.
American Journal of Diseases of Children (1960)|December 1, 1993
Risk of congenital heart defects in relatives of patients with atrioventricular canalM C Digilio, B Marino, M P Cicini, et al.
The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.
American Journal of Medical Genetics|November 7, 1998
Noonan syndrome and aortic coarctationM C Digilio, B Marino, F Picchio, et al.
Minerva Pediatrica|June 1, 1991
[The life style and physical activity of the child operated on for congenital cardiopathy]F Drago, M C Digilio, S Giannico, et al.
The American Journal of Cardiology|January 1, 1995
Transposition of the great arteries associated with deletion of chromosome 22q11S Melchionda, M C Digilio, R Mingarelli, et al.
Cytogenetic and Genome Research|August 17, 2005
Pure trisomy 19p syndrome in an infant with an extra ring chromosomeA Novelli, C Ceccarini, L Bernardini, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 13, 2000
Antigliadin and antiendomysial antibodies in children with Down's syndromeB Papadatou, F Ferretti, A Giannotti, et al.
Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, et al.
Pageof 13