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B MARINO

Showing results (81-90 of 428) with videos related to

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Clinical Genetics|November 18, 2003
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome)M C Digilio, A Giannotti, B Dallapiccola, et al.
British Heart Journal|September 1, 1994
Familial atrioventricular septal defect: possible genetic mechanismM C Digilio, B Marino, A Giannotti, et al.
Pediatric Cardiology|May 8, 2014
Surgical outcomes for patients with Turner syndromeP Versacci, L M Silvestri, S Maiolo, et al.
American Journal of Medical Genetics|January 31, 1998
Familial deletions of chromosome 22q11M C Digilio, B Marino, A Giannotti, et al.
The Journal of Cardiovascular Surgery|April 9, 2001
Aortopulmonary window coexisting with tetralogy of FallotD Alborino, P Guccione, R Di Donato, et al.
American Journal of Medical Genetics|February 13, 1995
Maternal diabetes causing DiGeorge anomaly and renal agenesisM C Digilio, B Marino, R Formigari, et al.
American Journal of Medical Genetics|January 10, 1997
The atrioventricular canal defect is the congenital heart disease connecting short rib-polydactyly and oral-facial-digital syndromesM C Digilio, B Marino, A Giannotti, et al.
Archives of Disease in Childhood|January 1, 1997
Chromosome 22q11 microdeletion and isolated conotruncal heart defectsM C Digilio, B Marino, A Giannotti, et al.
Pediatric Cardiology|January 1, 1997
Atrioventricular canal defect and postaxial polydactyly indicating phenotypic overlap of Ellis-van Creveld and Kaufman-McKusick syndromesM C Digilio, B Marino, A Giannotti, et al.
Chest|December 1, 1989
Atrioventricular canal associated with trisomy 9B Marino, M C Digilio, A Giannotti, et al.
Pageof 43

Showing results (81-90 of 428) with videos related to

Sort By:
Pageof 43
Clinical Genetics|November 18, 2003
Postural anomaly of the head-neck-shoulder alignment in patients with deletion 22q11.2 (DiGeorge/velocardiofacial syndrome)M C Digilio, A Giannotti, B Dallapiccola, et al.
British Heart Journal|September 1, 1994
Familial atrioventricular septal defect: possible genetic mechanismM C Digilio, B Marino, A Giannotti, et al.
Pediatric Cardiology|May 8, 2014
Surgical outcomes for patients with Turner syndromeP Versacci, L M Silvestri, S Maiolo, et al.
American Journal of Medical Genetics|January 31, 1998
Familial deletions of chromosome 22q11M C Digilio, B Marino, A Giannotti, et al.
The Journal of Cardiovascular Surgery|April 9, 2001
Aortopulmonary window coexisting with tetralogy of FallotD Alborino, P Guccione, R Di Donato, et al.
American Journal of Medical Genetics|February 13, 1995
Maternal diabetes causing DiGeorge anomaly and renal agenesisM C Digilio, B Marino, R Formigari, et al.
American Journal of Medical Genetics|January 10, 1997
The atrioventricular canal defect is the congenital heart disease connecting short rib-polydactyly and oral-facial-digital syndromesM C Digilio, B Marino, A Giannotti, et al.
Archives of Disease in Childhood|January 1, 1997
Chromosome 22q11 microdeletion and isolated conotruncal heart defectsM C Digilio, B Marino, A Giannotti, et al.
Pediatric Cardiology|January 1, 1997
Atrioventricular canal defect and postaxial polydactyly indicating phenotypic overlap of Ellis-van Creveld and Kaufman-McKusick syndromesM C Digilio, B Marino, A Giannotti, et al.
Chest|December 1, 1989
Atrioventricular canal associated with trisomy 9B Marino, M C Digilio, A Giannotti, et al.
Pageof 43