Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature-Reference-Cited by-同舟云学术

Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature

Published:2014-02 Issue:2 Volume:43 Page:139-146
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

de wit M. C.¹,Srebniak M. I.²,Govaerts L. C. P.²,Van Opstal D.²,Galjaard R. J. H.²,Go A. T. J. I.¹

Affiliation:

1. Department of Obstetrics and Gynecology; Erasmus Medical Centre; Rotterdam The Netherlands

2. Department of Clinical Genetics; Erasmus Medical Centre; Rotterdam The Netherlands

Publisher

Wiley

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/uog.12575/fullpdf

Reference45 articles.

1. Ultrasonographically detectable markers of fetal chromosomal abnormalities;Nicolaides;Lancet,1992

2. Distribution of abnormal karyotypes among malformed fetuses detected by ultrasound throughout gestation;Rizzo;Prenat Diagn,1996

3. Ultrasound diagnosis of fetal abnormalities and cytogenetic evaluation;Zalen-Sprock;Prenat Diagn,1991

4. Detection of large-scale variation in the human genome;Iafrate;Nat Genet,2004

5. Global variation in copy number in the human genome;Redon;Nature,2006

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