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                             10 gevonden resultaten
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
                             10 gevonden resultaten
 
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