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Maria Cristina Digilio

Showing results (31-40 of 232) with videos related to

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American Journal of Medical Genetics. Part A|December 22, 2015
Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature reviewGiulio Calcagni, Anwar Baban, Enrica De Luca, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 30, 2016
Congenital heart defects in Noonan syndrome and RIT1 mutationGiulio Calcagni, Anwar Baban, Francesca Romana Lepri, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
European Journal of Pediatrics|April 17, 2002
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomaliesAlessandra Toscano, Silvia Anaclerio, Maria Cristina Digilio, et al.
Developmental Disabilities Research Reviews|July 19, 2008
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndromeAdriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, et al.
Developmental Medicine and Child Neurology|October 5, 2022
Epilepsy in KBG syndromeMarina Auconi, Domenico Serino, Maria Cristina Digilio, et al.
Birth Defects Research|July 8, 2024
Partial atrioventricular canal defect and aortic coarctation associated with variants in GDF1 and NOTCH1 genes: A case reportCarolina Putotto, Marco Masci, Monia Magliozzi, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome)Maria Cristina Digilio, Aldo Giannotti, Massimo Castro, et al.
American Journal of Medical Genetics. Part A|April 1, 2004
Ellis-van Creveld Syndrome with hydrometrocolpos is not linked to chromosome arm 4p or 20pMaria Cristina Digilio, Isabella Torrente, Judith A Goodship, et al.
Pageof 24

Showing results (31-40 of 232) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part A|December 22, 2015
Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature reviewGiulio Calcagni, Anwar Baban, Enrica De Luca, et al.
Italian Journal of Pediatrics|May 15, 2020
Genetics of atrioventricular canal defectsFlaminia Pugnaloni, Maria Cristina Digilio, Carolina Putotto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 30, 2016
Congenital heart defects in Noonan syndrome and RIT1 mutationGiulio Calcagni, Anwar Baban, Francesca Romana Lepri, et al.
Giornale Italiano Di Cardiologia (2006)|February 8, 2013
[Congenital heart diseases in women]Carolina Putotto, Marta Unolt, Angela Caiaro, et al.
European Journal of Pediatrics|April 17, 2002
Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomaliesAlessandra Toscano, Silvia Anaclerio, Maria Cristina Digilio, et al.
Developmental Disabilities Research Reviews|July 19, 2008
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndromeAdriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, et al.
Developmental Medicine and Child Neurology|October 5, 2022
Epilepsy in KBG syndromeMarina Auconi, Domenico Serino, Maria Cristina Digilio, et al.
Birth Defects Research|July 8, 2024
Partial atrioventricular canal defect and aortic coarctation associated with variants in GDF1 and NOTCH1 genes: A case reportCarolina Putotto, Marco Masci, Monia Magliozzi, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome)Maria Cristina Digilio, Aldo Giannotti, Massimo Castro, et al.
American Journal of Medical Genetics. Part A|April 1, 2004
Ellis-van Creveld Syndrome with hydrometrocolpos is not linked to chromosome arm 4p or 20pMaria Cristina Digilio, Isabella Torrente, Judith A Goodship, et al.
Pageof 24