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Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

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Robinson,  P. N.
Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Citation

Robinson, P. N. (2010). Whole-exome sequencing for finding de novo mutations in sporadic mental retardation. Genome Biology, 11(12), 11:144-11:144. doi:10.1186/gb-2010-11-12-144.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-79BF-B
Abstract
Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.