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Q37001689-5F406275-1D63-4BF6-B1E3-266F52D5DF21
Q37001689-5F406275-1D63-4BF6-B1E3-266F52D5DF21
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http://www.wikidata.org/entity/statement/Q37001689-5F406275-1D63-4BF6-B1E3-266F52D5DF21
Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report.
P2860
Q37001689-5F406275-1D63-4BF6-B1E3-266F52D5DF21
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37001689-5F406275-1D63-4BF6-B1E3-266F52D5DF21
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b479731b71de373503656a1d0fdbb0df86371f73
P2860
The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects.