| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
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
|
Millar, David S
|
|
2010
|
4 |
6 |
p. 384-393
|
artikel
|
| 2 |
ArrayTrack: a free FDA bioinformatics tool to support emerging biomedical research -- an update
|
Xu, Joshua
|
|
2010
|
4 |
6 |
p. 428-434
|
artikel
|
| 3 |
A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
|
Karimpour-Fard, Anis
|
|
2010
|
4 |
6 |
p. 421-427
|
artikel
|
| 4 |
Color Atlas of Pharmacology
|
Konstandi, Maria
|
|
2010
|
4 |
6 |
|
artikel
|
| 5 |
Endothelial nitric oxide synthase gene polymorphisms -786T >C and 894G >T in coronary artery bypass graft surgery patients
|
Ragia, Georgia
|
|
2010
|
4 |
6 |
p. 375-383
|
artikel
|
| 6 |
Evolutionary divergence and functions of the human acyl-CoA thioesterase gene (ACOT) family
|
Brocker, Chad
|
|
2010
|
4 |
6 |
p. 411-420
|
artikel
|
| 7 |
General considerations for integrating pharmacogenomics into mainstream medical practice
|
Patrinos, George P
|
|
2010
|
4 |
6 |
p. 371-374
|
artikel
|
| 8 |
Intronic polymorphisms of cytochromes P450
|
Ingelman-Sundberg, Magnus
|
|
2010
|
4 |
6 |
p. 402-405
|
artikel
|
| 9 |
KinSNP software for homozygosity mapping of disease genes using SNP microarrays
|
Amir, El-Ad David
|
|
2010
|
4 |
6 |
p. 394-401
|
artikel
|
| 10 |
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
|
Cooper, David N
|
|
2010
|
4 |
6 |
p. 406-410
|
artikel
|
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