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Neeta L Vora

Showing results (31-40 of 97) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
A single center's experience with noninvasive prenatal testingCarmen J Beamon, Emily E Hardisty, Sarah C Harris, et al.
Prenatal Diagnosis|September 2, 2018
Ethical and counseling challenges in prenatal exome sequencingSarah Harris, Kelly Gilmore, Emily Hardisty, et al.
Prenatal Diagnosis|July 23, 2019
Fetal phenotypes emerge as genetic technologies become robustKathryn J Gray, Louise E Wilkins-Haug, Nancy J Herrig, et al.
Prenatal Diagnosis|May 6, 2025
Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys-Dietz SyndromeMia B Hodges, Sally Harris, Brianna Murphy, et al.
Obstetrical & Gynecological Survey|August 17, 2016
Cell-Free DNA Screening: Complexities and Challenges of Clinical ImplementationMatthew R Grace, Emily Hardisty, Sarah K Dotters-Katz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2024
Disparities in access to reproductive genetic services associated with geographic location of residence and maternal race and ethnicityAsha N Talati, Divya P Mallampati, Emily E Hardisty, et al.
Clinical Therapeutics|June 5, 2026
Prenatal Diagnosis and Novel Therapeutics in Treatment of Genetic Conditions: Challenges and OpportunitiesAsha N Talati, Maura Jones, Emily E Hardisty, et al.
O&G Open|September 26, 2025
Addressing Barriers to Autopsy and Genetic Testing in Stillbirth WorkupKaren J Gibbins, Neeta L Vora, Akila Subramaniam, et al.
American Journal of Obstetrics and Gynecology|May 10, 2015
Cell free DNA testing-interpretation of results using an online calculatorMatthew R Grace, Emily Hardisty, Noah S Green, et al.
Prenatal Diagnosis|February 8, 2022
Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosisAsha N Talati, Kelly L Gilmore, Emily E Hardisty, et al.
Pageof 10

Showing results (31-40 of 97) with videos related to

Sort By:
Pageof 10
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
A single center's experience with noninvasive prenatal testingCarmen J Beamon, Emily E Hardisty, Sarah C Harris, et al.
Prenatal Diagnosis|September 2, 2018
Ethical and counseling challenges in prenatal exome sequencingSarah Harris, Kelly Gilmore, Emily Hardisty, et al.
Prenatal Diagnosis|July 23, 2019
Fetal phenotypes emerge as genetic technologies become robustKathryn J Gray, Louise E Wilkins-Haug, Nancy J Herrig, et al.
Prenatal Diagnosis|May 6, 2025
Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys-Dietz SyndromeMia B Hodges, Sally Harris, Brianna Murphy, et al.
Obstetrical & Gynecological Survey|August 17, 2016
Cell-Free DNA Screening: Complexities and Challenges of Clinical ImplementationMatthew R Grace, Emily Hardisty, Sarah K Dotters-Katz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2024
Disparities in access to reproductive genetic services associated with geographic location of residence and maternal race and ethnicityAsha N Talati, Divya P Mallampati, Emily E Hardisty, et al.
Clinical Therapeutics|June 5, 2026
Prenatal Diagnosis and Novel Therapeutics in Treatment of Genetic Conditions: Challenges and OpportunitiesAsha N Talati, Maura Jones, Emily E Hardisty, et al.
O&G Open|September 26, 2025
Addressing Barriers to Autopsy and Genetic Testing in Stillbirth WorkupKaren J Gibbins, Neeta L Vora, Akila Subramaniam, et al.
American Journal of Obstetrics and Gynecology|May 10, 2015
Cell free DNA testing-interpretation of results using an online calculatorMatthew R Grace, Emily Hardisty, Noah S Green, et al.
Prenatal Diagnosis|February 8, 2022
Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosisAsha N Talati, Kelly L Gilmore, Emily E Hardisty, et al.
Pageof 10