Characterizing the phenotypic effect of Xq28 duplication size inMECP2duplication syndrome-Reference-Cited by-同舟云学术

Characterizing the phenotypic effect of Xq28 duplication size inMECP2duplication syndrome

Published:2019-03-15 Issue:5 Volume:95 Page:575-581
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Peters Sarika U.¹^ORCID,Fu Cary¹,Suter Bernhard²,Marsh Eric³,Benke Timothy A.⁴,Skinner Steve A.⁵,Lieberman David N.⁶,Standridge Shannon⁷,Jones Mary⁸,Beisang Arthur⁹,Feyma Timothy⁹,Heydeman Peter¹⁰,Ryther Robin¹¹,Kaufmann Walter E.¹²,Glaze Daniel G.²,Neul Jeffrey L.¹,Percy Alan K.¹³

Affiliation:

1. Department of PediatricsVanderbilt University Medical Center Nashville Tennessee

2. Department of PediatricsBaylor College of Medicine Houston Texas

3. Division of Neurology and PediatricsChildren's Hospital of Philadelphia Philadelphia Pennsylvania

4. Department of PediatricsUniversity of Colorado School of Medicine Aurora Colorado

5. Greenwood Genetic Center Greenwood South Carolina

6. Department of PediatricsBoston Children's Hospital Boston Massachusetts

7. Department of PediatricsCincinnati Children's Hospital Cincinnati Ohio

8. Department of Pediatrics, UCSF Benioff Children's Hospital Oakland California

9. Department of PediatricsGilette Children's Specialty Healthcare Saint Paul Minnesota

10. Department of PediatricsRush University Medical Center Chicago Illinois

11. Department of Neurology, Washington University School of Medicine St. Louis Missouri

12. Dept. Human Genetics, Emory University School of Medicine

13. Department of Pediatrics, University of Alabama at Birmingham Birmingham Alabama

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13521

Reference36 articles.

1. Genomic disorders ten years on

2. MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription

3. MeCP2 as an Activator of Gene Expression

4. Autism and other neuropsychiatric symptoms are prevalent in individuals withMeCP2duplication syndrome

5. MECP2 duplication syndrome;Van Esch H;Mol Syndromol,2012

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