X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation
<p>Abstract</p> <p>Background</p> <p>Aproximately 5–10% of cases of mental retardation in males are due to copy number variations (CNV) on the X chromosome. Novel technologies, such as array comparative genomic hybridization (aCGH), may help to uncover cryptic rearrange...
Main Authors: | , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2007-11-01
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Series: | BMC Genomics |
Online Access: | http://www.biomedcentral.com/1471-2164/8/443 |