Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound-Reference-Cited by-同舟云学术

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound

Published:2012-07-30 Issue:10 Volume:32 Page:986-995
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Shaffer Lisa G.¹,Rosenfeld Jill A.¹,Dabell Mindy P.¹,Coppinger Justine¹,Bandholz Anne M.¹,Ellison Jay W.¹,Ravnan J. Britt¹,Torchia Beth S.¹,Ballif Blake C.¹,Fisher Allan J.²

Affiliation:

1. Signature Genomic Laboratories, PerkinElmer, Inc. Spokane Washington USA

2. Commonwealth Perinatal Services Richmond Virginia USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.3943

Reference32 articles.

1. Ultrasonographically detectable markers of fetal chromosomal abnormalities

2. Ultrasound screening for fetal chromosome anomalies

3. Prospective ranking of the sonographic markers for aneuploidy: Data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound

4. Changes in the Utilization of Prenatal Diagnosis

5. Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?

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