Microduplication of 3p26.3 Implicated in Cognitive Development
We report here a 34-month-old boy with global developmental delay referred for molecular karyotyping and fragile X studies. Molecular karyotype analysis revealed a microduplication in the 3p26.3 region involving part of the CHL1 and CNTN6 genes. Several deletions, one translocation, and one duplicat...
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Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
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Series: | Case Reports in Genetics |
Online Access: | http://dx.doi.org/10.1155/2014/295359 |
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