6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies

6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies

<p>Abstract</p> <p>Background</p> <p>The interstitial 6p deletions, involving the 6p22-p24 chromosomal region, are rare events characterized by variable phenotypes and no clear genotype-phenotype correlation has been established so far.</p> <p>Results</p&...

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Bibliographic Details
Main Authors: Di Benedetto Daniela, Di Vita Giuseppa, Romano Corrado, Giudice Mariangela Lo, Vitello Girolamo Aurelio, Zingale Marinella, Grillo Lucia, Castiglia Lucia, Musumeci Sebastiano Antonino, Fichera Marco
Format: Article
Language:English
Published: BMC 2013-01-01
Series:Molecular Cytogenetics
Subjects:
6p22.3 deletion
Array-CGH
ASDs
Hypotonia
DTNBP1
Online Access:http://www.molecularcytogenetics.org/content/6/1/4

Internet

http://www.molecularcytogenetics.org/content/6/1/4

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