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Q24655227-0F44BFE4-BE2F-45F6-8C16-0A6184866DCB
Q24655227-0F44BFE4-BE2F-45F6-8C16-0A6184866DCB
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http://www.wikidata.org/entity/statement/Q24655227-0F44BFE4-BE2F-45F6-8C16-0A6184866DCB
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study
P2860
Q24655227-0F44BFE4-BE2F-45F6-8C16-0A6184866DCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24655227-0F44BFE4-BE2F-45F6-8C16-0A6184866DCB
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b2a664f5d6b2becba304dee9517ed5ea90e3167f
P2860
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox