Prenatal Diagnosis: Screening and Diagnostic Tools.
Carlson LM, Vora NL.
Obstet Gynecol Clin North Am. 2017 Jun;44(2):245-256. doi: 10.1016/j.ogc.2017.02.004.
Prenatal Screening for Microdeletions and Rare Autosomal Aneuploidies.
Fiorentino D, Dar P.
Clin Obstet Gynecol. 2023 Sep 1;66(3):579-594. doi: 10.1097/GRF.0000000000000799. Epub 2023 Jul 13.
Noninvasive prenatal screening for fetal sex chromosome aneuploidies.
Deng C, Cheung SW, Liu H.
Expert Rev Mol Diagn. 2021 Apr;21(4):405-415. doi: 10.1080/14737159.2021.1911651. Epub 2021 Apr 11.
Prenatal screening for genetic disorders: Suggested guidelines for the Indian Scenario.
Phadke SR, Puri RD, Ranganath P.
Indian J Med Res. 2017 Dec;146(6):689-699. doi: 10.4103/ijmr.IJMR_1788_15.
Current landscape of prenatal genetic screening and testing.
Krstić N, Običan SG.
Birth Defects Res. 2020 Mar 1;112(4):321-331. doi: 10.1002/bdr2.1598. Epub 2019 Oct 21.
Navigating Noninvasive Prenatal Screening for Subchromosomal Abnormalities.
Talati AN, Hardisty EE, Vora NL.
Am Fam Physician. 2022 Dec;106(6):612-613.
Prenatal diagnosis and management of omphalocele.
Verla MA, Style CC, Olutoye OO.
Semin Pediatr Surg. 2019 Apr;28(2):84-88. doi: 10.1053/j.sempedsurg.2019.04.007. Epub 2019 Apr 6.
Prenatal screening for haemoglobin disorders.
Petrou M, Modell B.
Prenat Diagn. 1995 Dec;15(13):1275-95. doi: 10.1002/pd.1970151308.
Guideline No. 456: Prenatal Screening for Fetal Chromosomal Anomalies.
Audibert F, Wou K, Okun N, De Bie I, Wilson RD.
J Obstet Gynaecol Can. 2024 Nov;46(11):102694. doi: 10.1016/j.jogc.2024.102694. Epub 2024 Oct 16.
Prenatal screening and diagnosis of aneuploidy in multiple pregnancies.
Gagnon A, Audibert F.
Best Pract Res Clin Obstet Gynaecol. 2014 Feb;28(2):285-94. doi: 10.1016/j.bpobgyn.2013.12.010. Epub 2013 Dec 31.
