Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report.
| Autor: | Haj, Roland1 HajR@shmc.org, Jackson, Kelly2 kelly.jackson@louisville.edu, Torchia, Beth A.1 torchia@signaturegenomics.com, Shaffer, Lisa G.1 shaffer@signaturegenomics.com, Bejjani, Bassem A.1 bejjani@signaturegenomics.com, Gowans, Gordon C.2 gcgowa01@louisville.edu, Ruff, Michael W.3 mwruff@insightbb.com |
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| Zdroj: | Molecular Cytogenetics (17558166). 2009, Vol. 2, p1-5. 5p. 3 Color Photographs, 1 Diagram, 2 Graphs. |
| Databáze: | Academic Search Ultimate |
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