Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study-Reference-Cited by-同舟云学术

Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study

Published:2018-12 Issue:6 Volume:52 Page:715-721
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Egloff M.¹²,Hervé B.³⁴,Quibel T.⁵,Jaillard S.⁶,Le Bouar G.⁷,Uguen K.⁸,Saliou A.‐H.⁹,Valduga M.¹⁰,Perdriolle E.¹¹,Coutton C.¹²,Coston A.‐L.¹³,Coussement A.¹⁴,Anselem O.¹⁵,Missirian C.¹⁶,Bretelle F.¹⁷,Prieur F.¹⁸,Fanget C.¹⁹,Muti C.²⁰,Jacquemot M.‐C.²¹,Beneteau C.²²,Le Vaillant C.²³,Vekemans M.¹²,Salomon L. J.²²⁴,Vialard F.³⁴,Malan V.¹²^ORCID

Affiliation:

1. Service d'Histologie‐Embryologie‐CytogénétiqueHôpital Necker‐Enfants Malades, APHP Paris France

2. Sorbonne Paris Cité, Université Paris Descartes Paris France

3. Unité de CytogénétiqueCHI de Poissy St Germain Poissy France

4. EA7404‐GIG, UFR des Sciences de la Santé Simone VeilUVSQ Montigny‐le‐Bretonneux France

5. Service de Gynécologie ObstétriqueCHI de Poissy St Germain Poissy France

6. Service de Cytogénétique et Biologie CellulaireCHU de Rennes Rennes France

7. Département de Gynécologie Obstétrique et Reproduction HumaineCHU de Rennes Rennes France

8. Laboratoire de Cytogénétique, Cytologie et Biologie de la ReproductionCHRU Brest France

9. Centre Pluridisciplinaire de Diagnostic PrénatalCHRU Brest France

10. Service de GénétiqueCHRU Nancy‐Brabois Nancy France

11. Service d'ObstétriqueCHRU Nancy‐Brabois Nancy France

12. Laboratoire de Génétique Chromosomique, INSERM 1209, CNRS UMR 5309, CHU Grenoble Alpes, Institut Albert BonniotUniversité Grenoble Alpes Grenoble France

13. Service de Gynécologie‐Obstétrique et Médecine de la ReproductionHôpital Couple Enfant, Université Grenoble Alpes, CHU Grenoble Alpes Grenoble France

14. Laboratoire de Cytogénétique, Hôpital CochinAPHP Paris France

15. Service de Gynécologie et Obstétrique de Port‐Royal, Maternité Port‐RoyalGroupe Hospitalier Cochin Broca Hôtel‐Dieu, APHP Paris France

16. Département de Génétique MédicaleCHU Timone Enfants, APHM Marseille France

17. Service de Gynécologie ObstétriqueCHU Nord, APHM Marseille France

18. Service de Génétique Clinique Chromosomique MoléculaireCHU Saint‐Etienne Saint‐Etienne France

19. Service d'ObstétriqueCHU Saint‐Etienne Saint‐Etienne France

20. Génétique Constitutionnelle, Laboratoire de BiologieCentre Hospitalier de Versailles Le Chesnay France

21. Consultation de Diagnostic Prénatal, Service de Gynécologie ObstétriqueCentre Hospitalier de Versailles Le Chesnay France

22. Service de Génétique MédicaleCHU Nantes Nantes France

23. Service de Gynécologie‐ObstétriqueCHU de Nantes Nantes France

24. Service d'ObstétriqueHôpital Necker‐Enfants Malades, APHP Paris France

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.18928

Reference34 articles.

1. Ultrasonographically detectable markers of fetal chromosomal abnormalities

2. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation

3. Pregnancy outcome in fetuses with increased nuchal translucency and normal karyotype

4. Increased nuchal translucency with normal karyotype

5. Risk of selected structural abnormalities in infants after increased nuchal translucency measurement

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