Association of Copy Number Variants With Specific Ultrasonographically Detected Fetal Anomalies-Reference-Cited by-同舟云学术

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Association of Copy Number Variants With Specific Ultrasonographically Detected Fetal Anomalies

Published:2014-07 Issue:1 Volume:124 Page:83-90
ISSN:0029-7844
Container-title:Obstetrics & Gynecology
language:en
Short-container-title:

Author:

Donnelly Jennifer C.,Platt Lawrence D.,Rebarber Andrei,Zachary Julia,Grobman William A.,Wapner Ronald J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Obstetrics and Gynaecology

Reference6 articles.

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

2. . Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.;Hillman;Ultrasound Obstet Gynecol,2013

3. . A copy number variation morbidity map of developmental delay.;Cooper;Nat Genet,2011

4. . Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.;Shaffer;Prenatal Diagn,2012

5. Committee Opinion No. 581. American College of Obstetricians and Gynecologists.;Obstet Gynecol,2013

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1. Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review;Heliyon;2024-09

2. Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study;Orphanet Journal of Rare Diseases;2024-08-22

3. Chromosomal abnormalities detected by chromosomal microarray analysis and pregnancy outcomes of 4211 fetuses with high-risk prenatal indications;Scientific Reports;2024-07-10

4. Clinical application of chromosomal microarray analysis in high-risk pregnancies;Gazzetta Medica Italiana Archivio per le Scienze Mediche;2024-07

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