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Marta Unolt

Showing results (21-30 of 34) with videos related to

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Plos One|April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in miceGioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
European Journal of Medical Genetics|November 21, 2022
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart diseaseCarolina Putotto, Marta Unolt, Caterina Lambiase, et al.
Journal of Medical Genetics|September 12, 2019
Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndromeMartina Fanella, Marianna Frascarelli, Caterina Lambiase, et al.
International Journal of Molecular Sciences|March 25, 2017
Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in TanzaniaSerena Caggiano, Nicola Ullmann, Elisa De Vitis, et al.
Clinical Genetics|December 8, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 DeletionsTanner J Nelson, Daniel E McGinn, T Blaine Crowley, et al.
Birth Defects Research|June 20, 2020
Atypical cardiac defects in patients with RASopathies: Updated data on CARNET studyGiulio Calcagni, Giulia Gagliostro, Giuseppe Limongelli, et al.
American Journal of Medical Genetics. Part A|November 1, 2018
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of PhiladelphiaIan M Campbell, Sarah E Sheppard, T Blaine Crowley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Plos One|April 2, 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in miceGioia Mastromoro, Giulio Calcagni, Paolo Versacci, et al.
American Journal of Medical Genetics. Part A|December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patientsMaria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
European Journal of Medical Genetics|November 21, 2022
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart diseaseCarolina Putotto, Marta Unolt, Caterina Lambiase, et al.
Journal of Medical Genetics|September 12, 2019
Myoclonic epilepsy, parkinsonism, schizophrenia and left-handedness as common neuropsychiatric features in 22q11.2 deletion syndromeMartina Fanella, Marianna Frascarelli, Caterina Lambiase, et al.
International Journal of Molecular Sciences|March 25, 2017
Factors That Negatively Affect the Prognosis of Pediatric Community-Acquired Pneumonia in District Hospital in TanzaniaSerena Caggiano, Nicola Ullmann, Elisa De Vitis, et al.
Clinical Genetics|December 8, 2025
Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 DeletionsTanner J Nelson, Daniel E McGinn, T Blaine Crowley, et al.
Birth Defects Research|June 20, 2020
Atypical cardiac defects in patients with RASopathies: Updated data on CARNET studyGiulio Calcagni, Giulia Gagliostro, Giuseppe Limongelli, et al.
American Journal of Medical Genetics. Part A|November 1, 2018
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of PhiladelphiaIan M Campbell, Sarah E Sheppard, T Blaine Crowley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndromeSólveig Óskarsdóttir, Erik Boot, Terrence Blaine Crowley, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
Pageof 4