| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genetic association study in the Gambia using tagging polymorphisms in the major histocompatibility complex class III region implicates a HLA-B associated transcript 2 polymorphism in severe malaria susceptibility
|
Diakite, Mahamadou
|
|
2008
|
125 |
1 |
p. 105-109
|
artikel
|
| 2 |
Associations of PLA2G7 gene polymorphisms with plasma lipoprotein-associated phospholipase A2 activity and coronary heart disease in a Chinese Han population: the Beijing atherosclerosis study
|
Hou, Liping
|
|
2008
|
125 |
1 |
p. 11-20
|
artikel
|
| 3 |
David N. Cooper and Hildegard Kehrer-Sawatzki (Eds.): Handbook of human molecular evolution
|
Cobb, Matthew
|
|
2008
|
125 |
1 |
p. 113-114
|
artikel
|
| 4 |
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31
|
Liu, Xue-Zhong
|
|
2008
|
125 |
1 |
p. 53-62
|
artikel
|
| 5 |
Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci
|
Lei, Shu-Feng
|
|
2008
|
125 |
1 |
p. 1-9
|
artikel
|
| 6 |
Identification of common genetic variants that account for transcript isoform variation between human populations
|
Zhang, Wei
|
|
2008
|
125 |
1 |
p. 81-93
|
artikel
|
| 7 |
Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects
|
Allen, Emily Graves
|
|
2008
|
125 |
1 |
p. 41-52
|
artikel
|
| 8 |
Moyra Smith: Translational research in genetics and genomics
|
Morrison, Patrick J.
|
|
2008
|
125 |
1 |
p. 115
|
artikel
|
| 9 |
Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene
|
Alías, Laura
|
|
2008
|
125 |
1 |
p. 29-39
|
artikel
|
| 10 |
Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission
|
Askland, Kathleen
|
|
2008
|
125 |
1 |
p. 63-79
|
artikel
|
| 11 |
Sonic hedgehog mutations identified in holoprosencephaly patients can act in a dominant negative manner
|
Singh, Samer
|
|
2008
|
125 |
1 |
p. 95-103
|
artikel
|
| 12 |
The association of SNPs in ADIPOQ, ADIPOR1, and ADIPOR2 with insulin sensitivity in a cohort of adolescents and their parents
|
Rasmussen-Torvik, Laura J.
|
|
2008
|
125 |
1 |
p. 21-28
|
artikel
|
| 13 |
The woman who walked into the sea: Huntington’s and the making of a genetic disease
|
Harper, Peter S.
|
|
2008
|
125 |
1 |
p. 111-112
|
artikel
|
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