Works matching IS 1434-5161 AND VI 49 AND IP 6 AND DT 2004
Results: 9
Reproductive attitudes of couples having a child with cystic fibrosis in Brittany (France).
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 285, doi. 10.1007/s10038-004-0147-2
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Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 312, doi. 10.1007/s10038-004-0146-3
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Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 290, doi. 10.1007/s10038-004-0148-1
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Polymorphisms of the prion protein gene (PRNP) in a Korean population.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 319, doi. 10.1007/s10038-004-0150-7
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Hydrocephalus and Hirschsprung’s disease with a mutation of L1CAM.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 334, doi. 10.1007/s10038-004-0153-4
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Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 302, doi. 10.1007/s10038-004-0151-6
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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 308, doi. 10.1007/s10038-004-0145-4
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D919G polymorphism of methionine synthase gene is associated with blood pressure response to benazepril in Chinese hypertensive patients.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 296, doi. 10.1007/s10038-004-0149-0
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Heterozygosities and allelic frequencies of 811 dinucleotide-repeat marker loci in the Taiwanese population.
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- Journal of Human Genetics, 2004, v. 49, n. 6, p. 325, doi. 10.1007/s10038-004-0152-5
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- Article