Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome

Published:2022-07 Issue:1 Volume:227 Page:79.e1-79.e11
ISSN:0002-9378
Container-title:American Journal of Obstetrics and Gynecology
language:en
Short-container-title:American Journal of Obstetrics and Gynecology

Author:

Dar Pe’er^ORCID,Jacobsson Bo,Clifton Rebecca,Egbert Melissa^ORCID,Malone Fergal,Wapner Ronald J.,Roman Ashley S.,Khalil Asma,Faro Revital,Madankumar Rajeevi,Edwards Lance,Strong Noel,Haeri Sina,Silver Robert,Vohra Nidhi,Hyett Jon^ORCID,Demko Zachary^ORCID,Martin Kimberly,Rabinowitz Matthew,Flood Karen,Carlsson Ylva^ORCID,Doulaveris Georgios^ORCID,Daly Sean,Hallingström Maria,MacPherson Cora,Kao Charlly,Hakonarson Hakon^ORCID,Norton Mary E.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference33 articles.

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3. Cell-free DNA analysis for noninvasive examination of trisomy;Norton;N Engl J Med,2015

4. Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing;Dar;Am J Obstet Gynecol,2014

5. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012

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2. Advancing fetal diagnosis and prognostication using comprehensive prenatal phenotyping and genetic testing;Pediatric Research;2024-06-27

3. Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context;Genetics in Medicine;2024-05

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5. High positive predictive value 22q11.2 microdeletion screening by prenatal cell‐free DNA testing that incorporates fetal fraction amplification;Prenatal Diagnosis;2024-04-15