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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

Roland Haj email, Kelly Jackson email, Beth A Torchia email, Lisa G Shaffer email, Bassem A Bejjani email, Gordon C Gowans email and Michael E Ruff email

Molecular Cytogenetics 2009, 2:2doi:10.1186/1755-8166-2-2

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