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A J Agopian

Showing results (121-130 of 134) with videos related to

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American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Medical Genetics. Part A|March 15, 2023
Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000-2017: A report from the National Birth Defects Prevention NetworkBailey A Martin-Giacalone, Angela E Lin, Sonja A Rasmussen, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.
American Journal of Human Genetics|June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation. Genomic and Precision Medicine|February 16, 2026
<i>ROBO2</i> Variants Associated With Atrial Septal Defect Define a Novel Regulatory ElementSeong Won Kim, Michael Parfenov, Laura Rodriguez-Murillo, et al.
Scientific Reports|July 21, 2021
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Human Molecular Genetics|January 29, 2019
The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulationYoussef A Kousa, Huiping Zhu, Walid D Fakhouri, et al.
Scientific Reports|October 23, 2020
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Birth Defects Research|April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention StudyTonia C Carter, Denise M Kay, Faith Pangilinan, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
American Journal of Medical Genetics. Part A|March 15, 2023
Prevalence and descriptive epidemiology of Turner syndrome in the United States, 2000-2017: A report from the National Birth Defects Prevention NetworkBailey A Martin-Giacalone, Angela E Lin, Sonja A Rasmussen, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.
American Journal of Human Genetics|June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approachArchana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation. Genomic and Precision Medicine|February 16, 2026
<i>ROBO2</i> Variants Associated With Atrial Septal Defect Define a Novel Regulatory ElementSeong Won Kim, Michael Parfenov, Laura Rodriguez-Murillo, et al.
Scientific Reports|July 21, 2021
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Human Molecular Genetics|January 29, 2019
The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulationYoussef A Kousa, Huiping Zhu, Walid D Fakhouri, et al.
Scientific Reports|October 23, 2020
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndromeCristina E Trevino, Aaron M Holleman, Holly Corbitt, et al.
Birth Defects Research|April 30, 2025
Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention StudyTonia C Carter, Denise M Kay, Faith Pangilinan, et al.
American Journal of Medical Genetics. Part A|March 21, 2023
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variantsPagna Sok, Aniko Sabo, Lynn M Almli, et al.
Pageof 14