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Maria Cristina Digilio

Showing results (71-80 of 232) with videos related to

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American Journal of Medical Genetics. Part A|March 17, 2007
Clinical lumping and molecular splitting of LEOPARD and NF1/NF1-Noonan syndromesAnna Sarkozy, Annalisa Schirinzi, Francesca Lepri, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairsMaria Cristina Digilio, Laura Bernardini, Rita Mingarelli, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 9, 2022
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndromeFederica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, et al.
American Journal of Medical Genetics. Part A|December 22, 2015
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndromeFrancesca Clementina Radio, Maria Cristina Digilio, Rossella Capolino, et al.
American Journal of Human Genetics|December 27, 2011
Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with Kabuki syndromeDamien Lederer, Bernard Grisart, Maria Cristina Digilio, et al.
Clinical Dysmorphology|March 15, 2006
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of FallotPasquale Vergara, Maria Cristina Digilio, Andrea De Zorzi, et al.
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2014
Behavioral phenotype in Costello syndrome with atypical mutation: a case reportPaolo Alfieri, Cristina Caciolo, Giorgia Piccini, et al.
Frontiers in Physiology|July 24, 2019
<i>Trichoderma atroviride</i> P1 Colonization of Tomato Plants Enhances Both Direct and Indirect Defense Barriers Against InsectsMariangela Coppola, Pasquale Cascone, Ilaria Di Lelio, et al.
Pageof 24

Showing results (71-80 of 232) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part A|March 17, 2007
Clinical lumping and molecular splitting of LEOPARD and NF1/NF1-Noonan syndromesAnna Sarkozy, Annalisa Schirinzi, Francesca Lepri, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairsMaria Cristina Digilio, Laura Bernardini, Rita Mingarelli, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 9, 2022
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndromeFederica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, et al.
American Journal of Medical Genetics. Part A|December 22, 2015
Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndromeFrancesca Clementina Radio, Maria Cristina Digilio, Rossella Capolino, et al.
American Journal of Human Genetics|December 27, 2011
Deletion of KDM6A, a histone demethylase interacting with MLL2, in three patients with Kabuki syndromeDamien Lederer, Bernard Grisart, Maria Cristina Digilio, et al.
Clinical Dysmorphology|March 15, 2006
Genetic heterogeneity and phenotypic anomalies in children with atrioventricular canal defect and tetralogy of FallotPasquale Vergara, Maria Cristina Digilio, Andrea De Zorzi, et al.
Disease Markers|July 2, 2010
Multiplex ligation-dependent probe amplification analysis of GATA4 gene copy number variations in patients with isolated congenital heart diseaseValentina Guida, Francesca Lepri, Raymon Vijzelaar, et al.
American Journal of Medical Genetics. Part A|August 20, 2013
JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of FallotMaria Cristina Digilio, Alessandro De Luca, Francesca Lepri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2014
Behavioral phenotype in Costello syndrome with atypical mutation: a case reportPaolo Alfieri, Cristina Caciolo, Giorgia Piccini, et al.
Frontiers in Physiology|July 24, 2019
<i>Trichoderma atroviride</i> P1 Colonization of Tomato Plants Enhances Both Direct and Indirect Defense Barriers Against InsectsMariangela Coppola, Pasquale Cascone, Ilaria Di Lelio, et al.
Pageof 24