Research ArticleHUMAN GENETICS

Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders

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Science Advances  20 Feb 2019:
Vol. 5, no. 2, eaau9425
DOI: 10.1126/sciadv.aau9425

Article Information

vol. 5 no. 2

Online ISSN: 
History: 
  • Received for publication July 30, 2018
  • Accepted for publication January 9, 2019
  • .

Author Information

  1. Walid Abi Habib1,2,*,,
  2. Frédéric Brioude1,2,
  3. Salah Azzi1,2,
  4. Sylvie Rossignol3,
  5. Agnès Linglart4,5,
  6. Marie-Laure Sobrier1,
  7. Éloïse Giabicani1,2,
  8. Virginie Steunou1,
  9. Madeleine D. Harbison6,
  10. Yves Le Bouc1,2 and
  11. Irène Netchine1,2,
  1. 1Sorbonne Université, INSERM, UMRS 938, Centre de Recherche Saint-Antoine, Paris, France.
  2. 2AP-HP, Hôpital Trousseau, Service d’Explorations Fonctionnelles Endocriniennes, Paris, France.
  3. 3Service de Génétique Médicale, Centre de Référence pour les Anomalies du Développement (FECLAD), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  4. 4Endocrinology and Diabetology for Children and Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Bicêtre Paris Sud, AP-HP, Le Kremlin-Bicêtre, France.
  5. 5INSERM U986, INSERM, Le Kremlin-Bicêtre, France.
  6. 6Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  1. Corresponding author. Email: walid.abi-habib{at}inserm.fr (W.A.H.); irene.netchine{at}aphp.fr (I.N.)
  • * Present address: Center for Epigenetics, Van Andel Research Institute, Grand Rapids, MI, USA.

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