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Paula Goldenberg

Showing results (1-10 of 18) with videos related to

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Pediatric Annals|May 12, 2018
An Update on Common Chromosome Microdeletion and Microduplication SyndromesPaula Goldenberg
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 22, 2009
Evidence-based medicine and practice guidelines: application to geneticsHelga V Toriello, Paula Goldenberg
International Journal of Pediatric Otorhinolaryngology|February 21, 2019
Pharyngeal flap using carotid artery mobilization in 22q11.2 deletion syndrome with velopharyngeal insufficiencyMax Greenberg, Christen Caloway, Cheryl Hersh, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2019
Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associationsAngela E Lin, Stephanie Santoro, Frances A High, et al.
International Journal of Pediatric Otorhinolaryngology|December 28, 2020
Carotid artery mobilization prior to pharyngeal flap inset for patients with 22q11.2 deletion syndromeKrupa R Patel, Matthew Partain, Daniel P Ryan, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 1, 2013
Dilated cardiomyopathy in a 32-year-old woman with Russell-Silver syndromeThomas D Ryan, Anita Gupta, Divya Gupta, et al.
Cerebellum & Ataxias|March 24, 2018
Cerebellar cognitive affective syndrome: insights from Joubert syndromeChelsea L Hickey, Janet C Sherman, Paula Goldenberg, et al.
The Journal of Pediatrics|July 28, 2020
A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in InfancyAmy R Shikany, Benjamin J Landis, Ashley Parrott, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Aortopathy in the 7q11.23 microduplication syndromeAshley Parrott, Jeanne James, Paula Goldenberg, et al.
Frontiers in Genetics|May 28, 2021
Deep-Phenotyping the Less Severe Spectrum of <i>PIGT</i> Deficiency and Linking the Gene to Myoclonic Atonic SeizuresAllan Bayat, Manuela Pendziwiat, Ewa Obersztyn, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Pediatric Annals|May 12, 2018
An Update on Common Chromosome Microdeletion and Microduplication SyndromesPaula Goldenberg
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 22, 2009
Evidence-based medicine and practice guidelines: application to geneticsHelga V Toriello, Paula Goldenberg
International Journal of Pediatric Otorhinolaryngology|February 21, 2019
Pharyngeal flap using carotid artery mobilization in 22q11.2 deletion syndrome with velopharyngeal insufficiencyMax Greenberg, Christen Caloway, Cheryl Hersh, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2019
Congenital heart defects associated with aneuploidy syndromes: New insights into familiar associationsAngela E Lin, Stephanie Santoro, Frances A High, et al.
International Journal of Pediatric Otorhinolaryngology|December 28, 2020
Carotid artery mobilization prior to pharyngeal flap inset for patients with 22q11.2 deletion syndromeKrupa R Patel, Matthew Partain, Daniel P Ryan, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 1, 2013
Dilated cardiomyopathy in a 32-year-old woman with Russell-Silver syndromeThomas D Ryan, Anita Gupta, Divya Gupta, et al.
Cerebellum & Ataxias|March 24, 2018
Cerebellar cognitive affective syndrome: insights from Joubert syndromeChelsea L Hickey, Janet C Sherman, Paula Goldenberg, et al.
The Journal of Pediatrics|July 28, 2020
A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in InfancyAmy R Shikany, Benjamin J Landis, Ashley Parrott, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Aortopathy in the 7q11.23 microduplication syndromeAshley Parrott, Jeanne James, Paula Goldenberg, et al.
Frontiers in Genetics|May 28, 2021
Deep-Phenotyping the Less Severe Spectrum of <i>PIGT</i> Deficiency and Linking the Gene to Myoclonic Atonic SeizuresAllan Bayat, Manuela Pendziwiat, Ewa Obersztyn, et al.
Pageof 2