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Zachary Demko

Showing results (31-40 of 52) with videos related to

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Prenatal Diagnosis|October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociBernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Transplantation|March 28, 2024
Comparing Plasma Donor-derived Cell-free DNA to Gene Expression in Endomyocardial Biopsies in the Trifecta-Heart StudyPhilip F Halloran, Jeff Reeve, Martina Mackova, et al.
Transplantation Direct|April 13, 2026
Donor-derived Cell-free DNA for Detection of Rejection After Pancreas TransplantationAbraham J Matar, Samy Riad, Heidi Sarumi, et al.
Transplantation|April 10, 2024
Elevation of Donor-derived Cell-free DNA Before Biopsy-proven Rejection in Kidney TransplantJonathan S Bromberg, Suphamai Bunnapradist, Milagros Samaniego-Picota, et al.
Translational Oncology|October 27, 2015
Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR MethodologyEser Kirkizlar, Bernhard Zimmermann, Tudor Constantin, et al.
American Journal of Obstetrics and Gynecology|August 12, 2014
Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testingPe'er Dar, Kirsten J Curnow, Susan J Gross, et al.
Obstetrics and Gynecology|July 9, 2014
Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortEugene Pergament, Howard Cuckle, Bernhard Zimmermann, et al.
American Journal of Obstetrics and Gynecology|December 6, 2014
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromesRonald J Wapner, Joshua E Babiarz, Brynn Levy, et al.
American Journal of Obstetrics and Gynecology|March 25, 2023
Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening resultsMary E Norton, Cora MacPherson, Zachary Demko, et al.
Prenatal Diagnosis|December 9, 2023
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART studyKimberly Martin, Mary E Norton, Cora MacPherson, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Prenatal Diagnosis|October 31, 2012
Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociBernhard Zimmermann, Matthew Hill, George Gemelos, et al.
Transplantation|March 28, 2024
Comparing Plasma Donor-derived Cell-free DNA to Gene Expression in Endomyocardial Biopsies in the Trifecta-Heart StudyPhilip F Halloran, Jeff Reeve, Martina Mackova, et al.
Transplantation Direct|April 13, 2026
Donor-derived Cell-free DNA for Detection of Rejection After Pancreas TransplantationAbraham J Matar, Samy Riad, Heidi Sarumi, et al.
Transplantation|April 10, 2024
Elevation of Donor-derived Cell-free DNA Before Biopsy-proven Rejection in Kidney TransplantJonathan S Bromberg, Suphamai Bunnapradist, Milagros Samaniego-Picota, et al.
Translational Oncology|October 27, 2015
Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR MethodologyEser Kirkizlar, Bernhard Zimmermann, Tudor Constantin, et al.
American Journal of Obstetrics and Gynecology|August 12, 2014
Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testingPe'er Dar, Kirsten J Curnow, Susan J Gross, et al.
Obstetrics and Gynecology|July 9, 2014
Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortEugene Pergament, Howard Cuckle, Bernhard Zimmermann, et al.
American Journal of Obstetrics and Gynecology|December 6, 2014
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromesRonald J Wapner, Joshua E Babiarz, Brynn Levy, et al.
American Journal of Obstetrics and Gynecology|March 25, 2023
Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening resultsMary E Norton, Cora MacPherson, Zachary Demko, et al.
Prenatal Diagnosis|December 9, 2023
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART studyKimberly Martin, Mary E Norton, Cora MacPherson, et al.
Pageof 6