The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature-Reference-Cited by-同舟云学术

The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature

Published:2013-03-14 Issue:4 Volume:6 Page:268-279
ISSN:1939-3792
Container-title:Autism Research
language:en
Short-container-title:Autism Res

Author:

Urraca Nora¹,Cleary Julie²,Brewer Victoria³,Pivnick Eniko K.³⁴,McVicar Kathryn³,Thibert Ronald L.⁵,Schanen N. Carolyn⁶,Esmer Carmen⁷,Lamport Dustin⁸,Reiter Lawrence T.¹

Affiliation:

1. Department of Neurology University of Tennessee Health Science Center Memphis Tennessee

2. Department of Speech and Language Pathology University of Memphis Memphis Tennessee

3. Department of Pediatrics University of Tennessee Health Science Center Memphis Tennessee

4. Department of Ophthalmology University of Tennessee Health Science Center Memphis Tennessee

5. Department of Neurology Mass General Hospital Boston Massachusetts

6. Human Genetics Research Laboratory Nemours Biomedical Research Wilmington Delaware

7. Genetics Department Hospital Central “Dr. Ignacio Morones Prieto,” San Luis Potosí SLP Mexico

8. Department of Psychology University of South Alabama Mobile Alabama

Publisher

Wiley

Subject

Genetics(clinical),Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/aur.1284

Reference57 articles.

1. The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder

2. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)

3. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

4. Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

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