Reliable detection of subchromosomal deletions and duplications using cell‐based noninvasive prenatal testing

Author:

Vossaert Liesbeth1ORCID,Wang Qun1,Salman Roseen1,Zhuo Xinming1,Qu Chunjing2,Henke David1,Seubert Ron3,Chow Jennifer3,U'ren Lance3,Enright Brennan3,Stilwell Jackie34,Kaldjian Eric3,Yang Yaping12,Shaw Chad12,Levy Brynn5,Wapner Ronald6,Breman Amy1,Van den Veyver Ignatia17,Beaudet Arthur1ORCID

Affiliation:

1. Department of Molecular and Human GeneticsBaylor College of Medicine Houston TX USA

2. Baylor Genetics Laboratory Houston TX USA

3. RareCyte Inc. Seattle WA USA

4. Immune Design Seattle WA USA

5. Department of Pathology and Cell BiologyColumbia University Medical Center New York NY USA

6. Department of Obstetrics and GynecologyColumbia University Medical Center New York NY USA

7. Department of Obstetrics and GynecologyBaylor College of Medicine Houston TX USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference20 articles.

1. American College of Obstetricians and Gynecologists.ACOG committee opinion. [Internet]. American College of Obstetricians and Gynecologists; Accessed:https://www.acog.org/Resources‐And‐Publications/Committee‐Opinions/Committee‐on‐Genetics/Cell‐free‐DNA‐Screening‐for‐Fetal‐Aneuploidy

2. Practice Bulletin No. 163 Summary

3. Review: Cell-free fetal DNA in the maternal circulation as an indication of placental health and disease

4. Discordant non-invasive prenatal testing (NIPT) - a systematic review

5. Utilization of noninvasive prenatal testing: impact on referrals for diagnostic testing

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