Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing-Reference-Cited by-同舟云学术

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing

Published:2014-10-28 Issue:1 Volume:88 Page:25-31
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

van der Steen S.L.¹,Diderich K.E.M.¹,Riedijk S.R.¹,Verhagen-Visser J.¹,Govaerts L.C.P.¹,Joosten M.¹,Knapen M.F.C.M.²³,Van Opstal D.¹,Srebniak M.I.¹,Tibben A.⁴,Galjaard R.J.H.¹

Affiliation:

1. Department of Clinical Genetics

2. Department of Obstetrics and Prenatal Medicine; Erasmus Medical Centre; Rotterdam the Netherlands

3. Foundation of Prenatal Screening South-West; Rotterdam the Netherlands

4. Department Clinical Genetics; Leiden University Medical Centre; Leiden the Netherlands

Funder

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands

Foundation of Prenatal Screening South-West Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference24 articles.

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

2. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases;Fiorentino;Prenat Diagn,2011

3. How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?;Hillman;J Matern Fetal Neonatal Med,2013

4. Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature;Wit;Ultrasound Obstet Gynecol,2014

5. Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification;Srebniak;Eur J Hum Genet,2014

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