Molecular basis of congenital Lp(a) deficiency: a frequent apo(a) ‘null’ mutation in Caucasians

By Ogorelkova Miroslava   Gruber Alexandra   Utermann Gerd  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2087-2096

Oxford University Press

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Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium

By Kraft H-G.   Windegger M.   Menzel H.J.   Utermann G.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 257-264

Oxford University Press

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Single nucleotide polymorphisms in the human interleukin-1B gene affect transcription according to haplotype context

By Chen Hongmin   Wilkins Leon M.   Aziz Nazneen   Cannings Christopher   Wyllie David H.   Bingle Colin   Rogus John   Beck James D.   Offenbacher Steven   Cork Michael J.   Rafie-Kolpin Maryam   Hsieh Chung-Ming   Kornman Kenneth S.   Duff Gordon W.  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 519-529

Oxford University Press

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Single-nucleotide polymorphisms in porcine mannan-binding lectin A

By Lillie Brandon   Keirstead Natalie   Squires E.   Hayes M.  

Immunogenetics, Vol. 58, Iss. 12, 2006-12 ,pp. : 983-993

Springer Publishing Company

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Single nucleotide polymorphisms as tools in human genetics

By Gray Ian C.   Campbell DavidA.   Spurr NigelK.  

Human Molecular Genetics, Vol. 9, Iss. 16, 2000-10 ,pp. : 2403-2408

Oxford University Press

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