| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks
|
Kapoor, Manav
|
|
2013
|
132 |
10 |
p. 1141-1151
|
artikel
|
| 2 |
Association, interaction, and replication analysis of genes encoding serotonin transporter and 5-HT3 receptor subunits A and B in alcohol dependence
|
Seneviratne, Chamindi
|
|
2013
|
132 |
10 |
p. 1165-1176
|
artikel
|
| 3 |
Early medical genetics in Soviet Russia: its growth and destruction
|
Harper, Peter S.
|
|
2013
|
132 |
10 |
p. 1193-1196
|
artikel
|
| 4 |
Responses to booster hepatitis B vaccination are significantly correlated with genotypes of human leukocyte antigen (HLA)-DPB1 in neonatally vaccinated adolescents
|
Wu, Tzu-Wei
|
|
2013
|
132 |
10 |
p. 1131-1139
|
artikel
|
| 5 |
The adaptive variant EDARV370A is associated with straight hair in East Asians
|
Tan, Jingze
|
|
2013
|
132 |
10 |
p. 1187-1191
|
artikel
|
| 6 |
The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability
|
Vandewalle, Joke
|
|
2013
|
132 |
10 |
p. 1177-1185
|
artikel
|
| 7 |
The new sequencer on the block: comparison of Life Technology’s Proton sequencer to an Illumina HiSeq for whole-exome sequencing
|
Boland, Joseph F.
|
|
2013
|
132 |
10 |
p. 1153-1163
|
artikel
|
| 8 |
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease
|
Cooper, David N.
|
|
2013
|
132 |
10 |
p. 1077-1130
|
artikel
|
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