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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-79BF-B Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-79C0-5
Genre: Journal Article
Alternative Title : Genome Biol

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gb-2010-11-12-144.pdf (Any fulltext), 284KB
 
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 Creators:
Robinson, P. N.1, Author           
Affiliations:
1Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              

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 Abstract: Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

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Language(s): eng - English
 Dates: 2010-12-21
 Publication Status: Issued
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 Identifiers: eDoc: 541926
URI: http://www.ncbi.nlm.nih.gov/pubmed/21172032
DOI: 10.1186/gb-2010-11-12-144
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Title: Genome Biology
  Alternative Title : Genome Biol
Source Genre: Journal
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Pages: - Volume / Issue: 11 (12) Sequence Number: - Start / End Page: 11:144 - 11:144 Identifier: ISSN: 1465-6906