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Q36549606-07D50C42-EAC6-47AA-9306-CEC8E047B686
Q36549606-07D50C42-EAC6-47AA-9306-CEC8E047B686
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http://www.wikidata.org/entity/statement/Q36549606-07D50C42-EAC6-47AA-9306-CEC8E047B686
Reciprocal changes in DNA methylation and hydroxymethylation and a broad repressive epigenetic switch characterize FMR1 transcriptional silencing in fragile X syndrome
P2860
Q36549606-07D50C42-EAC6-47AA-9306-CEC8E047B686
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36549606-07D50C42-EAC6-47AA-9306-CEC8E047B686
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wasDerivedFrom
b60f704b7e31059dde1a557b7df437f443cb9e99
P2860
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox