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Q35195742-0072B4FB-C60D-46FD-B56B-89FBE21B64FC
Q35195742-0072B4FB-C60D-46FD-B56B-89FBE21B64FC
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http://www.wikidata.org/entity/statement/Q35195742-0072B4FB-C60D-46FD-B56B-89FBE21B64FC
Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)
P2860
Q35195742-0072B4FB-C60D-46FD-B56B-89FBE21B64FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35195742-0072B4FB-C60D-46FD-B56B-89FBE21B64FC
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wasDerivedFrom
28d60cd5a3839fd9d3bec7ea6b8770bb99682171
P2860
Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.