Works matching IS 10184813 AND DT 2002 AND VI 10 AND IP 9
Results: 11
Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 569, doi. 10.1038/sj.ejhg.5200849
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Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 562, doi. 10.1038/sj.ejhg.5200848
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High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 553, doi. 10.1038/sj.ejhg.5200847
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Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 547, doi. 10.1038/sj.ejhg.5200844
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A genome scan for loci influencing anti-atherogenic serum bilirubin levels.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 539, doi. 10.1038/sj.ejhg.5200842
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The mutation spectrum of hyperphenylalanineaemia in the Republic of Ireland: the population history of the Irish revisited.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 530, doi. 10.1038/sj.ejhg.5200841
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Different genetic components inthe Norwegian population revealed by the analysis of mtDNA and Y chromosome polymorphisms.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 521, doi. 10.1038/sj.ejhg.5200834
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Gaucher disease in Romanian patients: incidence of the most common mutations and phenotypic manifestations.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 511, doi. 10.1038/sj.ejhg.5200845
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Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutationi detection (EMD).
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 505, doi. 10.1038/sj.ejhg.5200825
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A complex DNA-repeat structure within the Selenoprotein P promoter contains a functionally relevant polymorphism and is genetically unstable under conditions of mismatch repair deficiency.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 499, doi. 10.1038/sj.ejhg.5200811
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Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 516, doi. 10.1038/sj.ejhg.5200846
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- Article