Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?-Reference-Cited by-同舟云学术

Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?

Published:2019-08-19 Issue:11 Volume:39 Page:986-992
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Moradkhani Kamran¹^ORCID,Cuisset Laurence²,Boisseau Pierre¹,Pichon Olivier¹,Lebrun Marine³,Hamdi‐Rozé Houda⁴,Maurin Marie‐Laure⁵,Gruchy Nicolas⁶,Manca‐Pellissier Marie‐Christine⁷,Malzac Perrine⁷,Bilan Frédéric⁸,Audrezet Marie‐Pierre⁹,Saugier‐Veber Pascale¹⁰,Fauret‐Amsellem Anne‐Laure¹¹,Missirian Chantal⁷,Kuentz Paul¹²^ORCID,Egea Gregory¹³,Guichet Agnès¹⁴,Creveaux Isabelle¹⁵,Janel Caroline¹⁵,Harzallah Ines³,Touraine Renaud³,Goumy Carole¹⁶¹⁷,Joyé Nicole¹⁸,Puechberty Jacques¹⁹,Haquet Emmanuelle¹⁹,Chantot‐Bastaraud Sandra²⁰,Schmitt Sébastien¹,Gosset Philippe²¹,Duban‐Bedu Bénédicte²²,Delobel Bruno²²,Vago Philippe¹⁶¹⁷,Vialard François²³²⁴,Gomes Denise Molina²³²⁴,Siffroi Jean‐Pierre¹⁸,Bonnefont Jean‐Paul⁵,Dupont Jean‐Michel²⁵,Jonveaux Philippe²⁶,Doco‐Fenzy Martine²⁷,Sanlaville Damien²⁸²⁹,Le Caignec Cédric¹

Affiliation:

1. Service de Génétique MédicaleCHU Nantes Nantes France

2. Laboratory of Genetics and Molecular Biology, Institute Cochin and Cochin Hospital, APHPParis Descartes University Paris France

3. Service de Génétique–Laboratoire de Biologie MoléculaireCHU‐Hôpital Nord Saint‐Etienne France

4. Department of Molecular Genetics and GenomicsCHU Rennes Rennes France

5. Service d'Histologie, Embryologie, Cytogénétique.Groupe Hospitalier Necker‐Enfants Malades Paris France

6. Service de Génétique, CHU CaenUniversité Caen Normandie Caen France

7. Département de Génétique MédicaleAssistance Publique‐ Hôpitaux de Marseille Marseille France

8. Service de GénétiqueCHU de Poitiers Poitiers France

9. Laboratoire de Génétique MoléculaireCHRU, INSERM U1078 Brest France

10. Department of Genetics, Normandy Centre for Genomic Medicine and Personalized MedicineRouen University Hospital Rouen France

11. Department of GeneticsRobert‐Debré Teaching Hospital, Assistance Publique‐Hôpitaux de Paris Paris France

12. Génétique Biologique HistologieCentre Hospitalier Universitaire de Besançon Besançon France

13. Laboratoire de Biologie Médicale GEN‐BIO Clermont‐Ferrand France

14. Service de GénétiqueCHU Angers Angers France

15. Department of Biochemistry and Molecular GeneticsCHU Clermont‐Ferrand Clermont‐Ferrand France

16. Cytogénétique MédicaleCHU Estaing Clermont‐Ferrand France

17. U1240 Imagerie Moléculaire et Stratégies ThéranostiquesUniversité Clermont Auvergne, INSERM Clermont‐Ferrand France

18. Physiopathologie des Maladies Génétiques d'Expression PédiatriqueSorbonne Université, INSERM Paris France

19. Département de Génétique Médicale, Maladies Rares et Médecine PersonnaliséeHôpital Arnaud de Villeneuve, CHU de Montpellier Montpellier France

20. Physiopathologie des Maladies Génétiques d'Expression PédiatriqueINSERM Paris France

21. Diagnostic Préimplantatoire, Laboratoire de Diagnostic GénétiqueHôpitaux Universitaires de Strasbourg Strasbourg France

22. Centre de Génétique ChromosomiqueGH de l'Institut Catholique de Lille—Hopital Saint Vincent de Paul Lille France

23. Unité de CytogénétiqueCHI de Poissy St Germain en Laye Poissy France

24. EA7404‐GIGUFR des Sciences de la Santé Simone Veil, UVSQ Montigny‐le‐Bretonneux France

25. Laboratoire de CytogénétiqueHUPC Hôpital Cochin, APHP; Université Paris Descartes Paris France

26. Laboratoire de Génétique, CHRU Nancy, Inserm U1256Université de Lorraine Nancy France

27. Service de GénétiqueCHU REIMS, EA3801, UFR de Médecine REIMS Reims France

28. Department of GeneticsLyon University Hospitals Lyon France

29. Claude Bernard Lyon I University; Lyon Neuroscience Research Centre, CNRS UMR5292INSERM Lyon France

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5518

Reference32 articles.

1. American College of Medical Genetics Statement on Diagnostic Testing for Uniparental Disomy

2. CYTOGENETIC AND AGE-DEPENDENT RISK FACTORS ASSOCIATED WITH UNIPARENTAL DISOMY 15

3. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age

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