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[DOI] [PubMed] [Google Scholar] 151.Cao K., Stack D.E., Ramanathan R., Gross M.L., Rogan E.G., Cavalieri E.L

Although no single gene alteration has been found that explains all the features of PWS, several unique translocation and deletion patients have narrowed a key region to explain much of the PWS phenotype to the HBII-85 snoRNA gene (reviewed in Sahoo et al )

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