| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
|
Borck, Guntram
|
|
2010
|
129 |
1 |
p. 45-50
|
artikel
|
| 2 |
A novel survival multifactor dimensionality reduction method for detecting gene–gene interactions with application to bladder cancer prognosis
|
Gui, Jiang
|
|
2010
|
129 |
1 |
p. 101-110
|
artikel
|
| 3 |
−13915*G DNA polymorphism associated with lactase persistence in Africa interacts with Oct-1
|
Olds, Lynne C.
|
|
2010
|
129 |
1 |
p. 111-113
|
artikel
|
| 4 |
Genetic variants in the KIF6 region and coronary event reduction from statin therapy
|
Li, Yonghong
|
|
2010
|
129 |
1 |
p. 17-23
|
artikel
|
| 5 |
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16
|
Chapman, Nicola H.
|
|
2010
|
129 |
1 |
p. 59-70
|
artikel
|
| 6 |
Genome-wide analysis of copy number variants in age-related macular degeneration
|
Meyer, Kacie J.
|
|
2010
|
129 |
1 |
p. 91-100
|
artikel
|
| 7 |
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21
|
Piret, Sian E.
|
|
2010
|
129 |
1 |
p. 51-58
|
artikel
|
| 8 |
Heather Skirton and Christine Patch: Genetics for the health sciences: a handbook for clinical healthcare
|
Thistlewood, Helen
|
|
2010
|
129 |
1 |
p. 115
|
artikel
|
| 9 |
Mechanisms for phenotypic variation in Lesch–Nyhan disease and its variants
|
Sampat, Radhika
|
|
2010
|
129 |
1 |
p. 71-78
|
artikel
|
| 10 |
Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals
|
Janssen, Sabine
|
|
2010
|
129 |
1 |
p. 79-90
|
artikel
|
| 11 |
Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
|
Johansson, Åsa
|
|
2010
|
129 |
1 |
p. 25-34
|
artikel
|
| 12 |
Regions of homozygosity and their impact on complex diseases and traits
|
Ku, Chee Seng
|
|
2010
|
129 |
1 |
p. 1-15
|
artikel
|
| 13 |
Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach
|
Molina, Oscar
|
|
2010
|
129 |
1 |
p. 35-44
|
artikel
|
Tijdschrift beschrijving