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26. Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries. Futema M; Shah S; Cooper JA; Li K; Whittall RA; Sharifi M; Goldberg O; Drogari E; Mollaki V; Wiegman A; Defesche J; D'Agostino MN; D'Angelo A; Rubba P; Fortunato G; Waluś-Miarka M; Hegele RA; Aderayo Bamimore M; Durst R; Leitersdorf E; Mulder MT; Roeters van Lennep JE; Sijbrands EJ; Whittaker JC; Talmud PJ; Humphries SE Clin Chem; 2015 Jan; 61(1):231-8. PubMed ID: 25414277 [TBL] [Abstract][Full Text] [Related]
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30. Clinical utility gene card for: hyperlipoproteinemia, TYPE II. Kassner U; Wühle-Demuth M; Missala I; Humphries SE; Steinhagen-Thiessen E; Demuth I Eur J Hum Genet; 2014 Jul; 22(7):. PubMed ID: 24253857 [No Abstract] [Full Text] [Related]
31. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark. Jensen HK Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167 [TBL] [Abstract][Full Text] [Related]
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33. Spectrum of mutations of familial hypercholesterolemia in the 22 Arab countries. Alhababi D; Zayed H Atherosclerosis; 2018 Dec; 279():62-72. PubMed ID: 30415195 [TBL] [Abstract][Full Text] [Related]
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