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Q48061195-FB266DD9-13EC-4EFB-988B-D1AE8BCF7006
Q48061195-FB266DD9-13EC-4EFB-988B-D1AE8BCF7006
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http://www.wikidata.org/entity/statement/Q48061195-FB266DD9-13EC-4EFB-988B-D1AE8BCF7006
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells.
P2860
Q48061195-FB266DD9-13EC-4EFB-988B-D1AE8BCF7006
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48061195-FB266DD9-13EC-4EFB-988B-D1AE8BCF7006
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wasDerivedFrom
a1a7355bfaeca7864313d362af509c3aa7d08fa3
P2860
A mechanism for deletion formation in DNA by human cell extracts: the involvement of short sequence repeats.