Haplotype analysis of the CETP gene: not TaqIB, but the closely linked −629C→A polymorphism and a novel promoter variant are independently associated with CETP concentration

By Klerkx Anke H.E.M.  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-01 ,pp. : 111-123

Oxford University Press

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Functional inference of the methylenetetrahydrofolate reductase 677 C > T and 1298A > C polymorphisms from a large-scale epidemiological study

By Ulvik Arve   Ueland Per   Fredriksen Åse   Meyer Klaus   Vollset Stein   Hoff Geir   Schneede Jørn  

Human Genetics, Vol. 121, Iss. 1, 2007-03 ,pp. : 57-64

Springer Publishing Company

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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

By Caprioli Jessica   Castelletti Federica   Bucchioni Sara   Bettinaglio Paola   Bresin Elena   Pianetti Gaia   Gamba Sara   Brioschi Simona   Daina Erica   Remuzzi Giuseppe   for the International Registry of Recurrent and Familial HUS/TTP  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3385-3395

Oxford University Press

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Mutation –59c → t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia

By Scholtz Charlotte L.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2025-2030

Oxford University Press

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Cholesteryl Ester-Transfer Protein (CETP) Polymorphism and the Association of Acute Coronary Syndromes by Obesity Status in Greek Subjects: The CARDIO2000-GENE Study

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Human Heredity, Vol. 63, Iss. 3-4, 2007-02 ,pp. : 155-161

Karger

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