Single nucleotide polymorphism–based cell-free DNA prenatal screening for 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

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Single nucleotide polymorphism–based cell-free DNA prenatal screening for 22q11.2 deletion syndrome

Published:2022-07 Issue:1 Volume:227 Page:123-124
ISSN:0002-9378
Container-title:American Journal of Obstetrics and Gynecology
language:en
Short-container-title:American Journal of Obstetrics and Gynecology

Author:

Pan Min,Li Dong-Zhi

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference4 articles.

1. Expanding the indications for cell-free DNA in the maternal circulation: clinical considerations and implications;Di Renzo;Am J Obstet Gynecol,2019

2. Cell-free DNA analysis of maternal blood in prenatal screening for chromosomal microdeletions and microduplications: a systematic review;Familiari;Prenat Diagn,2021

3. Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome;Dar;Am J Obstet Gynecol,2022

4. The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies;Srebniak;Hum Mutat,2017

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