P713: Genome-wide cfDNA-based non-invasive prenatal screening for monogenic, chromosomal and sub-chromosomal disorders*

Genetics in Medicine Open 2026 Open access

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Authors: Noa Liscovitch‐Brauer, Jessica Giordano, Ronald WAPNER, Reut Tomashov Matar, Lina Basel‐Salmon, Ravit Mesika, Dolev Rahat, Sapir Sa'ar, Lilach Schneor, Shahar Shohat Koren, Gilad Magnazi, Noam Shomron
+6 more Hagit Daum, Lorinne Levitt, Amy Solnica, Dan Valsky, Nili Yanai, Drorith Hochner
DOI: 10.1016/j.gimo.2026.104205
Cited by: 0

Abstract

Methods: This retrospective cohort study included samples received for SNV-based prenatal cfDNA over a seven year period at a single commercial laboratory with an atypical result suggestive of BMT.Samples were analyzed as singleton non-egg donor or twin pregnancies.Samples were excluded if they were from individuals

Fields of Study & Subjects

Prenatal Screening and Diagnostics Assisted Reproductive Technology and Twin Pregnancy Genomics and Rare Diseases

Publication details

Journal / source
Genetics in Medicine Open
Volume
4
Pages
104205–104205
Publication date
1 January 2026
Language
EN