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Thomas Westover

Showing results (11-20 of 18) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 25, 2024
Fetal fraction amplification within prenatal cfDNA screening enables detection of genome-wide copy-number variants at enhanced resolutionAshley Acevedo, Oyang Teng, Heather G LaBreche, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|July 22, 2014
Standardized severe maternal morbidity review: rationale and processSarah J Kilpatrick, Cynthia Berg, Peter Bernstein, et al.
Obstetrics and Gynecology|July 9, 2014
Standardized severe maternal morbidity review: rationale and processSarah J Kilpatrick, Cynthia Berg, Peter Bernstein, et al.
Frontiers in Genetics|April 9, 2026
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT ConsortiumErica Soster, Kristin Dalton, Michael Bonifacio, et al.
European Journal of Human Genetics : EJHG|June 3, 2026
Health economic evaluations of genomic newborn screening: Approaches by studies within the international consortium on newborn sequencingHadley Stevens Smith, Martin Vu, Tamara Dangouloff, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2026
Ultrasound and SNP-based cell-free DNA zygosity testing in twin pregnanciesRuben Quintero, K Joseph Hurt, Neeta L Vora, et al.
American Journal of Obstetrics and Gynecology|February 18, 2015
Detection of microbial invasion of the amniotic cavity by analysis of cervicovaginal proteins in women with preterm labor and intact membranesC Andrew Combs, Thomas J Garite, Jodi A Lapidus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
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Showing results (11-20 of 18) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 25, 2024
Fetal fraction amplification within prenatal cfDNA screening enables detection of genome-wide copy-number variants at enhanced resolutionAshley Acevedo, Oyang Teng, Heather G LaBreche, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|July 22, 2014
Standardized severe maternal morbidity review: rationale and processSarah J Kilpatrick, Cynthia Berg, Peter Bernstein, et al.
Obstetrics and Gynecology|July 9, 2014
Standardized severe maternal morbidity review: rationale and processSarah J Kilpatrick, Cynthia Berg, Peter Bernstein, et al.
Frontiers in Genetics|April 9, 2026
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT ConsortiumErica Soster, Kristin Dalton, Michael Bonifacio, et al.
European Journal of Human Genetics : EJHG|June 3, 2026
Health economic evaluations of genomic newborn screening: Approaches by studies within the international consortium on newborn sequencingHadley Stevens Smith, Martin Vu, Tamara Dangouloff, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 19, 2026
Ultrasound and SNP-based cell-free DNA zygosity testing in twin pregnanciesRuben Quintero, K Joseph Hurt, Neeta L Vora, et al.
American Journal of Obstetrics and Gynecology|February 18, 2015
Detection of microbial invasion of the amniotic cavity by analysis of cervicovaginal proteins in women with preterm labor and intact membranesC Andrew Combs, Thomas J Garite, Jodi A Lapidus, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
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