Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in Iran-Reference-Cited by-同舟云学术

Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in Iran

Published:2019-09-05 Issue:3 Volume:47 Page:220-227
ISSN:1015-3837
Container-title:Fetal Diagnosis and Therapy
language:en
Short-container-title:Fetal Diagn Ther

Author:

Garshasbi Masoud,Wang Yicong^ORCID,Hantoosh Zadeh Sedigheh,Giti Sima,Piri Solmaz,Reza Hekmat Mohammad

Publisher

S. Karger AG

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference26 articles.

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4. Panburana P, Ajjimakorn S, Tungkajiwangoon P. First trimester Down Syndrome screening by nuchal translucency in a Thai population. Int J Gynaecol Obstet. 2001 Dec;75(3):311–2.

5. Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, et al. Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors. Prenat Diagn. 2012 Dec;32(13):1225–32.

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3. Relationships among maternal monosomy X mosaicism, maternal trisomy, and discordant sex chromosome aneuploidies;Clinica Chimica Acta;2024-02

4. Clinical evaluation of noninvasive prenatal testing for sex chromosome aneuploidies in 9,176 Korean pregnant women: a single-center retrospective study;BMC Pregnancy and Childbirth;2024-01-31

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