Noninvasive prenatal diagnosis for single gene disorders-Reference-Cited by-同舟云学术

Noninvasive prenatal diagnosis for single gene disorders

Published:2017-04 Issue:2 Volume:29 Page:73-79
ISSN:1040-872X
Container-title:Current Opinion in Obstetrics & Gynecology
language:en
Short-container-title:

Author:

Allen Stephanie,Young Elizabeth,Bowns Benjamin

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Obstetrics and Gynaecology

Reference39 articles.

1. Presence of fetal DNA in maternal plasma and serum;Lo;Lancet Lond Engl,1997

2. Prenatal diagnosis innovation: genome sequencing of maternal plasma;Wong;Annu Rev Med,2016

3. Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma;Xu;Genet Med,2015

4. Noninvasive prenatal diagnosis of Duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus;Yoo;Clin Chem,2015

5. Targeted sequencing of maternal plasma for haplotype-based noninvasive prenatal testing of spinal muscular atrophy;Chen;Ultrasound Obstet Gynecol,2016

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2. The current applications of cell-free fetal DNA in prenatal diagnosis of single-gene diseases: A review;International Journal of Reproductive BioMedicine (IJRM);2022-09-06

3. Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation;Genes;2022-08-24

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