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Seth I Berger

Showing results (21-30 of 61) with videos related to

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Clinical Therapeutics|February 4, 2026
Hereditary Anemias as a Monogenic Etiology for Nonimmune Hydrops FetalisMona M Makhamreh, Stephanie M Rice, Kavya Shivashankar, et al.
American Journal of Medical Genetics. Part A|December 29, 2023
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysisMona M Makhamreh, Kavya Shivashankar, Sarah Araji, et al.
Journal of Neuroscience Methods|June 12, 2012
Vamping: stereology-based automated quantification of fluorescent puncta size and densityDani Dumitriu, Seth I Berger, Carine Hamo, et al.
American Journal of Human Genetics|April 23, 2019
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with HoloprosencephalyPaul Kruszka, Seth I Berger, Karin Weiss, et al.
BMC Systems Biology|January 22, 2009
SNAVI: Desktop application for analysis and visualization of large-scale signaling networksAvi Ma'ayan, Sherry L Jenkins, Ryan L Webb, et al.
Prenatal Diagnosis|September 4, 2024
Prenatal Phenotype of Alkuraya-Kučinskas Syndrome: A Novel Case and Systematic Literature ReviewStephanie M Rice, Dante F Varotsis, Sascha Wodoslawsky, et al.
Obstetrics and Gynecology|November 4, 2021
Etiology and Outcome of Isolated Fetal Ascites: A Systematic ReviewRebecca Horgan, Julia A Youssef, Ariel T Levy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) StudyHuda B Al-Kouatly, Mona M Makhamreh, Stephanie M Rice, et al.
Congenital Anomalies|July 4, 2017
SIX3 deletions and incomplete penetrance in families affected by holoprosencephalyBethany Stokes, Seth I Berger, Beth A Hall, et al.
Biorxiv : the Preprint Server for Biology|February 19, 2024
Considerations for reporting variants in novel candidate genes identified during clinical genomic testingJessica X Chong, Seth I Berger, Samantha Baxter, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Clinical Therapeutics|February 4, 2026
Hereditary Anemias as a Monogenic Etiology for Nonimmune Hydrops FetalisMona M Makhamreh, Stephanie M Rice, Kavya Shivashankar, et al.
American Journal of Medical Genetics. Part A|December 29, 2023
RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysisMona M Makhamreh, Kavya Shivashankar, Sarah Araji, et al.
Journal of Neuroscience Methods|June 12, 2012
Vamping: stereology-based automated quantification of fluorescent puncta size and densityDani Dumitriu, Seth I Berger, Carine Hamo, et al.
American Journal of Human Genetics|April 23, 2019
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with HoloprosencephalyPaul Kruszka, Seth I Berger, Karin Weiss, et al.
BMC Systems Biology|January 22, 2009
SNAVI: Desktop application for analysis and visualization of large-scale signaling networksAvi Ma'ayan, Sherry L Jenkins, Ryan L Webb, et al.
Prenatal Diagnosis|September 4, 2024
Prenatal Phenotype of Alkuraya-Kučinskas Syndrome: A Novel Case and Systematic Literature ReviewStephanie M Rice, Dante F Varotsis, Sascha Wodoslawsky, et al.
Obstetrics and Gynecology|November 4, 2021
Etiology and Outcome of Isolated Fetal Ascites: A Systematic ReviewRebecca Horgan, Julia A Youssef, Ariel T Levy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) StudyHuda B Al-Kouatly, Mona M Makhamreh, Stephanie M Rice, et al.
Congenital Anomalies|July 4, 2017
SIX3 deletions and incomplete penetrance in families affected by holoprosencephalyBethany Stokes, Seth I Berger, Beth A Hall, et al.
Biorxiv : the Preprint Server for Biology|February 19, 2024
Considerations for reporting variants in novel candidate genes identified during clinical genomic testingJessica X Chong, Seth I Berger, Samantha Baxter, et al.
Pageof 7