Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 5
Results: 7
A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 5, p. 230, doi. 10.1007/s10038-005-0243-y
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- Article
Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene ( POMC) with low bone mineral density in adult women.
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- Journal of Human Genetics, 2005, v. 50, n. 5, p. 235, doi. 10.1007/s10038-005-0244-x
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- Article
Size of the protein-coding genome and rate of molecular evolution.
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- Journal of Human Genetics, 2005, v. 50, n. 5, p. 217, doi. 10.1007/s10038-005-0242-z
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- Article
Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.
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- Journal of Human Genetics, 2005, v. 50, n. 5, p. 264, doi. 10.1007/s10038-005-0246-8
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- Article
Assessment of tailor-made prevention of atherosclerosis with folic acid supplementation: randomized, double-blind, placebo-controlled trials in each MTHFR C677T genotype.
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- Journal of Human Genetics, 2005, v. 50, n. 5, p. 241, doi. 10.1007/s10038-005-0247-7
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- Article
Highly polymorphic human CYP4A11 gene.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 5, p. 259, doi. 10.1007/s10038-005-0245-9
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- Article
Discovery of genetic difference between asthmatic children with high IgE level and normal IgE level by whole genome linkage disequilibrium mapping using 763 autosomal STR markers.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 5, p. 249, doi. 10.1007/s10038-005-0248-6
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- Article