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The most recent version of this article was published on 1 January 2009

J Med Genet. Published Online First: 26 August 2008. doi:10.1136/jmg.2008.060871
Copyright © 2008 by the BMJ Publishing Group Ltd.

Review article

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

Carla Lintas 1 and Antonio M Persico 1*

1 University Campus Bio-Medico, Italy

* To whom correspondence should be addressed. E-mail: a.persico{at}unicampus.it.

Accepted 8 July 2008


Abstract

Autism spectrum disorders represent a group of developmental disorders with strong genetic underpinnings. Several cytogenetic abnormalities or de novo mutations able to cause autism have recently been uncovered. We have reviewed the Literature to highlight genotype-phenotype correlations between causal gene mutations or cytogenetic abnormalities and behavioral or morphological phenotypes. Based on this information, we propose a set of practical guidelines to help clinical geneticists pursue targeted genetic testing for autistic patients whose clinical phenotype is suggestive of a specific genetic or genomic etiology.


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This article has been cited by other articles:

  • O'Hare, A. (2009). Autism spectrum disorder: diagnosis and management. EDUCATION AND PRACTICE 94: 161-168 [Abstract] [Full Text]  

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