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Science Translational Medicine
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September 1, 2017
Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, et al.
Clinical Chemistry
|
June 2, 2021
Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies
Mark D Pertile, Nicola Flowers, Darcy Vavrek, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
May 21, 2003
Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound
Art Daniel, Neil Athayde, Robert Ogle, et al.
Prenatal Diagnosis
|
January 9, 2023
Performance of a cell-free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low-risk cell-free DNA screening
Katrina L Scarff, Nicola Flowers, Clare J Love, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
April 3, 2014
A novel combination of homeobox genes is expressed in mesenchymal chorionic stem/stromal cells in first trimester and term pregnancies
Haiying Liu, Padma Murthi, Sharon Qin, et al.
Placenta
|
March 20, 2016
Establishment and characterization of fetal and maternal mesenchymal stem/stromal cell lines from the human term placenta
Sharon Q Qin, Gina D Kusuma, Batla Al-Sowayan, et al.
Prenatal Diagnosis
|
October 5, 2020
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies
Glenn E Palomaki, Rossa W K Chiu, Mark D Pertile, et al.
The Journal of Obstetrics and Gynaecology Research
|
February 14, 2018
A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin
Anita Sik Yau Kan, Elizabeth Tak Kwong Lau, Chun Hong So, et al.
American Journal of Medical Genetics. Part A
|
November 16, 2006
High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy
Damien L Bruno, Trent Burgess, Hua Ren, et al.
Case Reports in Genetics
|
February 28, 2015
Exceptional complex chromosomal rearrangements in three generations
Hannie Kartapradja, Nanis Sacharina Marzuki, Mark D Pertile, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Science Translational Medicine
|
September 1, 2017
Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, et al.
Clinical Chemistry
|
June 2, 2021
Performance of a Paired-End Sequencing-Based Noninvasive Prenatal Screening Test in the Detection of Genome-Wide Fetal Chromosomal Anomalies
Mark D Pertile, Nicola Flowers, Darcy Vavrek, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
May 21, 2003
Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound
Art Daniel, Neil Athayde, Robert Ogle, et al.
Prenatal Diagnosis
|
January 9, 2023
Performance of a cell-free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low-risk cell-free DNA screening
Katrina L Scarff, Nicola Flowers, Clare J Love, et al.
Reproductive Sciences (Thousand Oaks, Calif.)
|
April 3, 2014
A novel combination of homeobox genes is expressed in mesenchymal chorionic stem/stromal cells in first trimester and term pregnancies
Haiying Liu, Padma Murthi, Sharon Qin, et al.
Placenta
|
March 20, 2016
Establishment and characterization of fetal and maternal mesenchymal stem/stromal cell lines from the human term placenta
Sharon Q Qin, Gina D Kusuma, Batla Al-Sowayan, et al.
Prenatal Diagnosis
|
October 5, 2020
International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies
Glenn E Palomaki, Rossa W K Chiu, Mark D Pertile, et al.
The Journal of Obstetrics and Gynaecology Research
|
February 14, 2018
A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin
Anita Sik Yau Kan, Elizabeth Tak Kwong Lau, Chun Hong So, et al.
American Journal of Medical Genetics. Part A
|
November 16, 2006
High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy
Damien L Bruno, Trent Burgess, Hua Ren, et al.
Case Reports in Genetics
|
February 28, 2015
Exceptional complex chromosomal rearrangements in three generations
Hannie Kartapradja, Nanis Sacharina Marzuki, Mark D Pertile, et al.
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of 4