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Research Title Research Type Research Year
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

 Article In Journal 1436
Research Title Research Type Research Year
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder

 Article In Journal 1436
Research Title Research Type Research Year
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome

 Article In Journal 1436

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No. of Records 3 records