General considerations for integrating pharmacogenomics into mainstream medical practice.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 371, doi. 10.1186/1479-7364-4-6-371
- Publication type:
- Article
Works matching IS 14739542 AND DT 2010 AND VI 4 AND IP 6
Results: 10
1
2
A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 421, doi. 10.1186/1479-7364-4-6-421
- Publication type:
- Article
3
An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 384, doi. 10.1186/1479-7364-4-6-384
- Publication type:
- Article
4
Evolutionary divergence and functions of the human acyl-CoA thioesterase gene (ACOT) family.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 411, doi. 10.1186/1479-7364-4-6-411
- Publication type:
- Article
5
Intronic polymorphisms of cytochromes P450.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 402, doi. 10.1186/1479-7364-4-6-402
- Publication type:
- Article
6
Color Atlas of Pharmacology.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 435, doi. 10.1186/1479-7364-4-6-435
- Publication type:
- Article
7
KinSNP software for homozygosity mapping of disease genes using SNP microarrays.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 394, doi. 10.1186/1479-7364-4-6-394
- Publication type:
- Article
8
Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotides.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 406, doi. 10.1186/1479-7364-4-6-406
- Publication type:
- Article
9
ArrayTrack: A free FDA bioinformatics tool to support emerging biomedical research -- An update.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 428, doi. 10.1186/1479-7364-4-6-428
- Publication type:
- Article
10
Endothelial nitric oxide synthase gene polymorphisms -786T > C and 894G > T in coronary artery bypass graft surgery patients.
- Published in:
- Human Genomics, 2010, v. 4, n. 6, p. 375, doi. 10.1186/1479-7364-4-6-375
- Publication type:
- Article