Works matching IS 14345161 AND DT 2000 AND VI 45 AND IP 5
Results: 12
Distribution of Δ32 alelle of the CCR5 gene in the population of Poland.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 271, doi. 10.1007/s100380070014
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Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 275, doi. 10.1007/s100380070015
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Association of the vitamin D receptor start codon polymorphism (FokI) with bone mineral density in postmenopausal Korean women.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 280, doi. 10.1007/s100380070016
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Genomic structure of the gene encoding human 3-hydroxy-3-methyl-glutaryl coenzyme A reductase: comparison of exon/intron organization of sterol-sensing domains among four related genes.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 284, doi. 10.1007/s100380070017
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The human ribosomal protein L6 gene in a critical region for Noonan syndrome.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 290, doi. 10.1007/s100380070018
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Association of essential hypertension in elderly Japanese with I/D polymorphism of the angiotensin-converting enzyme (ACE) gene.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 294, doi. 10.1007/s100380070019
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Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 299, doi. 10.1007/s100380070020
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Multiplex PCR amplification of TH01, D9S304, and D3S1744 loci.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 303, doi. 10.1007/s100380070021
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Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 305, doi. 10.1007/s100380070022
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cDNA cloning of a human RAB26-related gene encoding a Ras-like GTP-binding protein on chromosome 16p13.3 region.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 309, doi. 10.1007/s100380070023
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Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 315, doi. 10.1007/s100380070024
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cDNA cloning of a new member of the Ras superfamily, RAB9-like, on the human chromosome Xq22.1-q22.3 region.
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- Journal of Human Genetics, 2000, v. 45, n. 5, p. 318, doi. 10.1007/s100380070025
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