Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction-Reference-Cited by-同舟云学术

Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction

Published:2018-10-17 Issue:6 Volume:94 Page:575-580
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Petre Graciane¹²,Lorès Patrick³⁴⁵,Sartelet Hervé⁶,Truffot Aurélie⁷,Poreau Brice⁷,Brandeis Sandrine⁷,Martinez Guillaume⁷⁸,Satre Véronique²⁷⁸,Harbuz Radu⁷,Ray Pierre F.⁸⁹,Amblard Florence⁷,Devillard Françoise⁷,Vieville Gaëlle⁷,Berger Francois¹²,Jouk Pierre‐Simon²⁷,Vaiman Daniel³⁴⁵,Touré Aminata³⁴⁵,Coutton Charles²⁷⁸^ORCID,Bidart Marie¹²

Affiliation:

1. INSERM U1205UFR Chimie Biologie Grenoble France

2. Université Grenoble‐Alpes Grenoble France

3. INSERM U1016Institut Cochin Paris France

4. Centre National de la Recherche Scientifique UMR8104 Paris France

5. Faculté de MédecineUniversité Paris‐Descartes, Sorbonne Paris Cité Paris France

6. Département d'anatomie et cytologie pathologiquesCHU Grenoble‐Alpes Grenoble France

7. Département de Génétique et ProcréationCHU Grenoble‐Alpes Grenoble France

8. Equipe “Génétique, Epigénétique, Thérapies de l'Infertilité”IAB, INSERM 1209, CNRS UMR 5309 Grenoble France

9. Département de BiochimieToxicologie et Pharmacologie, UM GI‐DPI, CHU Grenoble‐Alpes Grenoble France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13449

Reference18 articles.

1. Intrauterine Growth Restriction: Hungry for an Answer

2. Intrauterine growth restriction—etiology and consequences: What do we know about the human situation and experimental animal models?☆

3. Fetal growth retardation: Associated malformations and chromosomal abnormalities

4. Intrauterine Growth Restriction (IUGR): Etiology and Diagnosis

5. The role of imprinted genes in humans

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