nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Adaptive evolution of loci covarying with the human African Pygmy phenotype
|
Mendizabal, Isabel |
|
2012 |
131 |
8 |
p. 1305-1317 |
artikel |
2 |
A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher
|
Meurs, Kathryn M. |
|
2012 |
131 |
8 |
p. 1319-1325 |
artikel |
3 |
Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events
|
Chiu, Shuenn-Nan |
|
2012 |
131 |
8 |
p. 1295-1304 |
artikel |
4 |
Further clarification of the contribution of the ADH1C gene to vulnerability of alcoholism and selected liver diseases
|
Li, Dawei |
|
2012 |
131 |
8 |
p. 1361-1374 |
artikel |
5 |
Genomic rearrangements at the FRA2H common fragile site frequently involve non-homologous recombination events across LTR and L1(LINE) repeats
|
Brueckner, Lena M. |
|
2012 |
131 |
8 |
p. 1345-1359 |
artikel |
6 |
Increased risk of stroke in oral contraceptive users carried replicated genetic variants: a population-based case–control study in China
|
Wang, Chun |
|
2012 |
131 |
8 |
p. 1337-1344 |
artikel |
7 |
McKinlay Gardner RJ, Sutherland GR, Shaffer LG: Chromosome abnormalities and genetic counselling
|
Barber, John C. K. |
|
2012 |
131 |
8 |
p. 1393-1394 |
artikel |
8 |
Mouse models of SMA: tools for disease characterization and therapeutic development
|
Bebee, Thomas W. |
|
2012 |
131 |
8 |
p. 1277-1293 |
artikel |
9 |
Reduced interferon (IFN)-α conditioned by IFNA2 (−173) and IFNA8 (−884) haplotypes is associated with enhanced susceptibility to severe malarial anemia and longitudinal all-cause mortality
|
Kempaiah, Prakasha |
|
2012 |
131 |
8 |
p. 1375-1391 |
artikel |
10 |
Using graded response model for the prediction of prostate cancer risk
|
Chen, Shyh-Huei |
|
2012 |
131 |
8 |
p. 1327-1336 |
artikel |