Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA-Reference-Cited by-同舟云学术

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA

Published:2014-12 Issue:6 Volume:211 Page:711-712
ISSN:0002-9378
Container-title:American Journal of Obstetrics and Gynecology
language:en
Short-container-title:American Journal of Obstetrics and Gynecology

Author:

Grati Francesca R.,Ferreira Jose C.P.B.^ORCID,Bajaj Komal

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference4 articles.

1. Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA;Porreco;Am J Obstet Gynecol,2014

2. Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results;Grati;Genet Med,2014

3. False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism;Gao;Ultrasound Obstet Gynecol,2014

4. Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotype;Srebniak;Ultrasound Obstet Gynecol,2014

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