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Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

DOI PDF Web Site 2 Citations

Journal

European Journal of Human Genetics

European Journal of Human Genetics 23 (2), 252-255, 2014-06-11

Springer Science and Business Media LLC

Citations (2)*help

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Details 詳細情報について

CRID

1360011144998767616
DOI

10.1038/ejhg.2014.103
ISSN

14765438

10184813
Web Site

http://www.nature.com/articles/ejhg2014103.pdf

http://www.nature.com/articles/ejhg2014103
Data Source
- Crossref

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