Last Updated: 09/26/2026
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Found 8 publications
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations.
Journal: Cytogenetic and genome research
Published: January 20, 2023
Autistic Disorder: A 20 Year Chronicle.
Journal: Journal of autism and developmental disorders
Published: June 28, 2020
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
Journal: European journal of human genetics : EJHG
Published: August 16, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: May 09, 2012
Clinical utility of the X-chromosome array.
Journal: American journal of medical genetics. Part A
Published: April 26, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome.
Journal: American journal of medical genetics. Part A
Published: February 13, 2012
Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders.
Journal: Molecular cytogenetics
Published: January 24, 2012
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Last Updated: 09/26/2026