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Neeta L Vora

Showing results (71-80 of 97) with videos related to

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Cells|July 14, 2023
A Shared Pathogenic Mechanism for Valproic Acid and <i>SHROOM3</i> Knockout in a Brain Organoid Model of Neural Tube DefectsTaylor N Takla, Jinghui Luo, Roksolana Sudyk, et al.
Prenatal Diagnosis|March 6, 2020
Lysosomal storage disease spectrum in nonimmune hydrops fetalis: a retrospective case control studyHuda B Al-Kouatly, Laura Felder, Mona M Makhamreh, et al.
Prenatal Diagnosis|October 5, 2020
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnanciesGlenn E Palomaki, Rossa W K Chiu, Mark D Pertile, et al.
JAMA|July 14, 2015
Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal MalignanciesDiana W Bianchi, Darya Chudova, Amy J Sehnert, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|November 23, 2022
Single-center serological surveillance of SARS-CoV-2 in pregnant patients presenting to labor and deliveryKim A Boggess, Elizabeth M Stringer, Whitney R Robinson, et al.
Plos One|December 18, 2018
Increasing the diagnostic yield of exome sequencing by copy number variant analysisDaniel S Marchuk, Kristy Crooks, Natasha Strande, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
American Journal of Medical Genetics. Part A|February 24, 2023
Diagnosis of TBC1D32-associated conditions: Expanding the phenotypic spectrum of a complex ciliopathySarah C Harris, Karen Chong, David Chitayat, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Cells|July 14, 2023
A Shared Pathogenic Mechanism for Valproic Acid and <i>SHROOM3</i> Knockout in a Brain Organoid Model of Neural Tube DefectsTaylor N Takla, Jinghui Luo, Roksolana Sudyk, et al.
Prenatal Diagnosis|March 6, 2020
Lysosomal storage disease spectrum in nonimmune hydrops fetalis: a retrospective case control studyHuda B Al-Kouatly, Laura Felder, Mona M Makhamreh, et al.
Prenatal Diagnosis|October 5, 2020
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnanciesGlenn E Palomaki, Rossa W K Chiu, Mark D Pertile, et al.
JAMA|July 14, 2015
Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal MalignanciesDiana W Bianchi, Darya Chudova, Amy J Sehnert, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|November 23, 2022
Single-center serological surveillance of SARS-CoV-2 in pregnant patients presenting to labor and deliveryKim A Boggess, Elizabeth M Stringer, Whitney R Robinson, et al.
Plos One|December 18, 2018
Increasing the diagnostic yield of exome sequencing by copy number variant analysisDaniel S Marchuk, Kristy Crooks, Natasha Strande, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 25, 2020
An approach to integrating exome sequencing for fetal structural anomalies into clinical practiceNeeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
American Journal of Medical Genetics. Part A|February 24, 2023
Diagnosis of TBC1D32-associated conditions: Expanding the phenotypic spectrum of a complex ciliopathySarah C Harris, Karen Chong, David Chitayat, et al.
Pageof 10