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Current Opinion in Pediatrics
|
September 12, 2014
Advances in genetic prenatal diagnosis and screening
Emily E Hardisty, Neeta L Vora
Obstetrics and Gynecology
|
July 23, 2014
In reply
Neeta L Vora, Barbara M O'Brien
American Journal of Obstetrics and Gynecology
|
August 26, 2022
Prenatal exome and genome sequencing for fetal structural abnormalities
Neeta L Vora, Mary E Norton
Seminars in Fetal & Neonatal Medicine
|
November 13, 2017
Screening for fetal chromosomal and subchromosomal disorders
Sarah Harris, Dallas Reed, Neeta L Vora
Prenatal Diagnosis
|
November 22, 2023
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Current Opinion in Obstetrics & Gynecology
|
January 8, 2025
Rho(D) immune globulin shortage and fetal Rh(D) screening with cell-free DNA
Matthew R Grace, Brighton Goodhue, Neeta L Vora
Prenatal Diagnosis
|
September 14, 2024
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
European Journal of Human Genetics : EJHG
|
April 26, 2026
Access alone does not define equity in reproductive genetics
Asha N Talati, Amy Mottola, Neeta L Vora
American Family Physician
|
December 15, 2022
Navigating Noninvasive Prenatal Screening for Subchromosomal Abnormalities
Asha N Talati, Emily E Hardisty, Neeta L Vora
Prenatal Diagnosis
|
April 22, 2020
Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic
Neeta L Vora, Emily Hardisty, Elizabeth Coviello, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 97) with videos related to
Sort By:
Page
of 10
Current Opinion in Pediatrics
|
September 12, 2014
Advances in genetic prenatal diagnosis and screening
Emily E Hardisty, Neeta L Vora
Obstetrics and Gynecology
|
July 23, 2014
In reply
Neeta L Vora, Barbara M O'Brien
American Journal of Obstetrics and Gynecology
|
August 26, 2022
Prenatal exome and genome sequencing for fetal structural abnormalities
Neeta L Vora, Mary E Norton
Seminars in Fetal & Neonatal Medicine
|
November 13, 2017
Screening for fetal chromosomal and subchromosomal disorders
Sarah Harris, Dallas Reed, Neeta L Vora
Prenatal Diagnosis
|
November 22, 2023
Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
Current Opinion in Obstetrics & Gynecology
|
January 8, 2025
Rho(D) immune globulin shortage and fetal Rh(D) screening with cell-free DNA
Matthew R Grace, Brighton Goodhue, Neeta L Vora
Prenatal Diagnosis
|
September 14, 2024
Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use"
Neeta L Vora, Sylvie Langlois, Lyn S Chitty
European Journal of Human Genetics : EJHG
|
April 26, 2026
Access alone does not define equity in reproductive genetics
Asha N Talati, Amy Mottola, Neeta L Vora
American Family Physician
|
December 15, 2022
Navigating Noninvasive Prenatal Screening for Subchromosomal Abnormalities
Asha N Talati, Emily E Hardisty, Neeta L Vora
Prenatal Diagnosis
|
April 22, 2020
Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic
Neeta L Vora, Emily Hardisty, Elizabeth Coviello, et al.
Page
of 10