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Amy E Roberts

Showing results (41-50 of 96) with videos related to

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Journal of the American Heart Association|December 16, 2015
Neuropsychological Status and Structural Brain Imaging in Adolescents With Single Ventricle Who Underwent the Fontan ProcedureDavid C Bellinger, Christopher G Watson, Michael J Rivkin, et al.
Nature Genetics|December 5, 2006
Germline gain-of-function mutations in SOS1 cause Noonan syndromeAmy E Roberts, Toshiyuki Araki, Kenneth D Swanson, et al.
American Journal of Human Genetics|April 22, 2008
TFAP2A mutations result in branchio-oculo-facial syndromeJeff M Milunsky, Tom A Maher, Geping Zhao, et al.
Cerebral Cortex (New York, N.Y. : 1991)|May 19, 2021
Abnormal Right-Hemispheric Sulcal Patterns Correlate with Executive Function in Adolescents with Tetralogy of FallotSarah U Morton, Lara Maleyeff, David Wypij, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 20, 2019
Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart DiseaseSarah U Morton, Lara Maleyeff, David Wypij, et al.
BMC Genomics|December 18, 2014
Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yieldJuan Geng, Jonathan Picker, Zhaojing Zheng, et al.
Heart Failure Clinics|November 15, 2021
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and ManagementMichele Lioncino, Emanuele Monda, Federica Verrillo, et al.
The Journal of Allergy and Clinical Immunology|September 6, 2025
Anifrolumab treatment of Singleton-Merten syndrome 2 due to a novel RIGI variantEvan E Hsu, Courtney E LeSon, Michael T Lam, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 5, 2024
Meta-regression of sulcal patterns, clinical and environmental factors on neurodevelopmental outcomes in participants with multiple CHD typesLara Maleyeff, Hannah J Park, Zahra S H Khazal, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple LentiginesEmanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Journal of the American Heart Association|December 16, 2015
Neuropsychological Status and Structural Brain Imaging in Adolescents With Single Ventricle Who Underwent the Fontan ProcedureDavid C Bellinger, Christopher G Watson, Michael J Rivkin, et al.
Nature Genetics|December 5, 2006
Germline gain-of-function mutations in SOS1 cause Noonan syndromeAmy E Roberts, Toshiyuki Araki, Kenneth D Swanson, et al.
American Journal of Human Genetics|April 22, 2008
TFAP2A mutations result in branchio-oculo-facial syndromeJeff M Milunsky, Tom A Maher, Geping Zhao, et al.
Cerebral Cortex (New York, N.Y. : 1991)|May 19, 2021
Abnormal Right-Hemispheric Sulcal Patterns Correlate with Executive Function in Adolescents with Tetralogy of FallotSarah U Morton, Lara Maleyeff, David Wypij, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 20, 2019
Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart DiseaseSarah U Morton, Lara Maleyeff, David Wypij, et al.
BMC Genomics|December 18, 2014
Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yieldJuan Geng, Jonathan Picker, Zhaojing Zheng, et al.
Heart Failure Clinics|November 15, 2021
Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and ManagementMichele Lioncino, Emanuele Monda, Federica Verrillo, et al.
The Journal of Allergy and Clinical Immunology|September 6, 2025
Anifrolumab treatment of Singleton-Merten syndrome 2 due to a novel RIGI variantEvan E Hsu, Courtney E LeSon, Michael T Lam, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 5, 2024
Meta-regression of sulcal patterns, clinical and environmental factors on neurodevelopmental outcomes in participants with multiple CHD typesLara Maleyeff, Hannah J Park, Zahra S H Khazal, et al.
Circulation. Genomic and Precision Medicine|May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple LentiginesEmanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
Pageof 10