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Bruno Dallapiccola

Showing results (11-20 of 454) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|January 28, 2014
Genetic insight into the pathogenesis of nonalcoholic fatty liver diseaseLuca Valenti, Bruno Dallapiccola, Valerio Nobili
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 defectsMaria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
European Journal of Medical Genetics|January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disordersEnza Maria Valente, Francesco Brancati, Bruno Dallapiccola
International Journal of Cardiology|March 3, 2007
Deletion 22q11 and isolated congenital heart diseaseM Cristina Digilio, Bruno Marino, Bruno Dallapiccola
American Journal of Medical Genetics. Part A|October 17, 2008
Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: a possible link to the Adams-Oliver syndromeM C Digilio, Bruno Marino, Bruno Dallapiccola
Heart (British Cardiac Society)|March 19, 2011
Screening for 22q11.2 microdeletion in adults with tetralogy of FallotM Cristina Digilio, Bruno Marino, Bruno Dallapiccola
American Journal of Medical Genetics. Part A|December 14, 2007
Autosomal dominant transmission of nonsyndromic diastasis recti and weakness of the linea albaM Cristina Digilio, Rossella Capolino, Bruno Dallapiccola
Handbook of Clinical Neurology|April 30, 2013
Joubert syndrome and related disordersEnza Maria Valente, Bruno Dallapiccola, Enrico Bertini
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 dysfunction536Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Pediatric Cardiology|March 7, 2012
Atrioventricular canal defect as a sign of laterality defect in Ellis-van Creveld and polydactyly syndromes with ciliary and Hedgehog signaling dysfunctionM Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Pageof 46

Showing results (11-20 of 454) with videos related to

Sort By:
Pageof 46
Journal of Pediatric Gastroenterology and Nutrition|January 28, 2014
Genetic insight into the pathogenesis of nonalcoholic fatty liver diseaseLuca Valenti, Bruno Dallapiccola, Valerio Nobili
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 defectsMaria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
European Journal of Medical Genetics|January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disordersEnza Maria Valente, Francesco Brancati, Bruno Dallapiccola
International Journal of Cardiology|March 3, 2007
Deletion 22q11 and isolated congenital heart diseaseM Cristina Digilio, Bruno Marino, Bruno Dallapiccola
American Journal of Medical Genetics. Part A|October 17, 2008
Autosomal dominant inheritance of aplasia cutis congenita and congenital heart defect: a possible link to the Adams-Oliver syndromeM C Digilio, Bruno Marino, Bruno Dallapiccola
Heart (British Cardiac Society)|March 19, 2011
Screening for 22q11.2 microdeletion in adults with tetralogy of FallotM Cristina Digilio, Bruno Marino, Bruno Dallapiccola
American Journal of Medical Genetics. Part A|December 14, 2007
Autosomal dominant transmission of nonsyndromic diastasis recti and weakness of the linea albaM Cristina Digilio, Rossella Capolino, Bruno Dallapiccola
Handbook of Clinical Neurology|April 30, 2013
Joubert syndrome and related disordersEnza Maria Valente, Bruno Dallapiccola, Enrico Bertini
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 dysfunction536Maria Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Pediatric Cardiology|March 7, 2012
Atrioventricular canal defect as a sign of laterality defect in Ellis-van Creveld and polydactyly syndromes with ciliary and Hedgehog signaling dysfunctionM Cristina Digilio, Bruno Dallapiccola, Bruno Marino
Pageof 46