Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 3
Results: 8
Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 118, doi. 10.1007/s10038-005-0230-3
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DNase II polymorphisms associated with risk of renal disorder among systemic lupus erythematosus patients.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 107, doi. 10.1007/s10038-004-0227-3
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Association analysis of signal transducer and activator of transcription 4 (STAT4) polymorphisms with asthma.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 133, doi. 10.1007/s10038-005-0232-1
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Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 151, doi. 10.1007/s10038-004-0228-2
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Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 124, doi. 10.1007/s10038-005-0231-2
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Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 112, doi. 10.1007/s10038-005-0229-9
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Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 155, doi. 10.1007/s10038-005-0233-0
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Parallel minisequencing followed by multiplex matrix-assisted laser desorption/ionization mass spectrometry assay for ß-thalassemia mutations.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 139, doi. 10.1007/s10038-005-0234-z
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- Article