A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia

Autism spectrum disorders (ASDs) are a heterogeneous group of disorders with unknown aetiology. Even though ASDs are suggested to be among the most heritable complex disorders, only a few reproducible mutations leading to susceptibility for ASD have been identified. In an attempt to identify ASD sus...

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Bibliographic Details
Main Author: Gilling, M. (author)
Other Authors: Lauritsen, M.B. (author), Møller, M. (author), Henriksen, K.F. (author), Vicente, A.M. (author), Oliveira, G. (author), Cintin, C. (author), Eiberg, H. (author), Andersen, P.S. (author), Mors, O. (author), Rosenberg, T. (author), Brøndum-Nielsen, K. (author), Cotterill, R.M. (author), Lundsteen, C. (author), Ropers, H.H. (author), Ullmann, R. (author), Bache, I. (author), Tümer, Z. (author), Tommerup, N. (author)
Format: article
Language:eng
Published: 2011
Subjects:
Translocation
Deletion
Autism
Myopia
Array CGH
Chromosome 18
Perturbações do Desenvolvimento Infantil e Saúde Mental
Online Access:http://hdl.handle.net/10400.18/313
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/313

Internet

http://hdl.handle.net/10400.18/313

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