4.2 Article

Significance of Low Maternal Serum B-hCG Levels in the Assessment of the Risk of Atypical Chromosomal Abnormalities

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations

Jing Wang et al.

Summary: The detection rate and positive predictive value of NIPS for fetal CNVs were approximately 51.1% and 19.7%, respectively. Follow-up molecular prenatal diagnosis is recommended for cases where NIPS suggests fetal CNVs.

FRONTIERS IN GENETICS (2021)

Article Obstetrics & Gynecology

Application of chromosomal microarray in fetuses with increased nuchal translucency

Xin-Rong Zhao et al.

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE (2020)

Article Acoustics

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis

M. M. Gil et al.

ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2017)

Article Acoustics

Chromosomal microarray in fetuses with increased nuchal translucency

I. C. B. Lund et al.

ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2015)

Article Obstetrics & Gynecology

Uptake of noninvasive prenatal testing at a large academic referral center

Sebastian Larion et al.

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2014)

Article Obstetrics & Gynecology

Chromosome Abnormalities Detected by Current Prenatal Screening and Noninvasive Prenatal Testing

Mary E. Norton et al.

OBSTETRICS AND GYNECOLOGY (2014)

Article Acoustics

Repeat measurements of nuchal translucency at 11-14 weeks of gestation: when do we need them?

L. J. Salomon et al.

ULTRASOUND IN OBSTETRICS & GYNECOLOGY (2013)

Article Obstetrics & Gynecology

First-trimester screening for chromosomal abnormalities

KH Nicolaides

SEMINARS IN PERINATOLOGY (2005)