Concepedia

Publication | Open Access

Unique and atypical deletions in Prader–Willi syndrome reveal distinct phenotypes

DOIFull Paper Access

105

Citations

30

References

2011

Year

Soo‐Jeong Kim, Jennifer Miller, Paul J. Kuipers, Jennifer R. German, Arthur L. Beaudet, Trilochan Sahoo, Daniel J. Driscoll
European Journal of Human Genetics

References

YearCitations

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