Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test-Reference-Cited by-同舟云学术

Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test

Published:2016-07-19 Issue:8 Volume:36 Page:760-765
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Janssens Katrien¹,Deiteren Kathleen²,Verlinden Anke³,Rooms Liesbeth⁴,Beckers Sigri⁴,Holmgren Philip⁴,Vermeulen Katrien²,Maes Marie-Berthe²,Mortier Geert¹⁴,Blaumeiser Bettina¹⁴

Affiliation:

1. Center of Medical Genetics; University of Antwerp; Wilrijk Belgium

2. Laboratory of Hematology; Antwerp University Hospital; Edegem Belgium

3. Department of Hematology; Antwerp University Hospital; Edegem Belgium

4. Center of Medical Genetics; Antwerp University Hospital; Edegem Belgium

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4857/fullpdf

Reference21 articles.

1. Introducing the non-invasive prenatal test for trisomy 21 in Belgium: a cost-consequences analysis;Neyt;BMJ Open,2014

3. The risk of fetal loss associated with invasive testing following combined first trimester risk screening for Down syndrome - a national cohort of 147987 singleton pregnancies;Wulff;Ultrasound Obstet Gynecol,2016

4. Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis;Gil;Ultrasound Obstet Gynecol,2015

5. Non-invasive detection of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advance stage Hodgkin's lymphoma by sequencing of circulating cell-free DNA: a technical proof-of-principle study;Vandenberghe;Lancet Haematol,2015

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