Results 111 to 120 of about 3,638 (166)

Noninvasive prenatal tests for chromosomal abnormality screening in in vitro fertilisation elderly pregnant women in northwest China. [PDF]

J Med Biochem
Xue S, Wang L, Yu Z, Zhu J, Feng L, Din G, Dai P.   +6 more
europepmc   +1 more source

Promoter landscape of maternal plasma DNA reveals predictive signatures of fetal growth restriction. [PDF]

Hum Genomics
Wang J, Du P, Wu Z, Zhao X, Hou F, Xin G, Du S, Kang J, Peng Y, Xu W, Jin H.   +10 more
europepmc   +1 more source

Identifying Differentially Methylated Sites for Methylation-Sensitive qPCR-based NIPT of Trisomies 13 and 18. [PDF]

Adv Biomed Res
Najafi A, Dastbaz E, Mehrabani A, Rajabi M, Sedaghat Shayegan G, Miryounesi M, Modarressi MH.   +6 more
europepmc   +1 more source

The Prediction of Pre-Eclampsia Using Low Fetal Fraction in a Machine Learning Model. [PDF]

Prenat Diagn
Wang J, Bai Y, Huang S, Lin Y, Ye S, Zhou W, Li S, Li N, Jiang M, Wang X.   +9 more
europepmc   +1 more source

NIPT and First Trimester Ultrasound [PDF]

Ultrasound in Medicine & Biology, 2017
openaire   +1 more source

Fetal fractions mediate the association between total cell-free DNA and preeclampsia risk in a non-invasive prenatal testing cohort. [PDF]

Hum Genomics
Zhang B, Chen X, Xi S, Zhan Z, Dong H, Zhang Y, Yuan X.   +6 more
europepmc   +1 more source

Patients' experiences using an educational virtual assistant for review of reproductive genetic screening results. [PDF]

J Genet Couns
Yarnall S, Saben JL, Sun N, Maisenbacher M, Shirazi T, Huda S, Falcone D, Parmar S.   +7 more
europepmc   +1 more source

NIPT-ohjaus perheen päätöksenteon tukena

, 2021
Suomalainen Merja, Manninen Minna, Kajula Outi   +2 more
openaire   +1 more source

Clinical Utility of Opportunistic Genome-Wide cfDNA Prenatal Screening in Intermediate-Risk Pregnancies. [PDF]

Genes (Basel)
Menao Guillén S, Pedrola L, Orellana C, Roselló M, Arruebo M, Lahuerta Pueyo C, Sobreviela Laserrada M, Marcos B, Pascual Mancho J, Cervera JV, Tajada M, Quiroga R.   +11 more
europepmc   +1 more source

Maternal mixed UPD3 and a homozygous PLXNA1 c.2497G>C variant in a fetus with severe anomalies. [PDF]

Front Med (Lausanne)
Ye Y, Wang X, He Y, Ning H, Zhang Z, Tao F, Zou Z, Fang Q, Chen Z, Tian X, Hao X.   +10 more
europepmc   +1 more source