| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12–q14
|
Kapoor, Ashish
|
|
2007
|
121 |
6 |
p. 655-662
|
artikel
|
| 2 |
Bivariate linkage confirms genetic contribution to fetal origins of childhood growth and cardiovascular disease risk in Hispanic children
|
Cai, Guowen
|
|
2007
|
121 |
6 |
p. 737-744
|
artikel
|
| 3 |
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies
|
Vissers, L. E. L. M.
|
|
2007
|
121 |
6 |
p. 697-709
|
artikel
|
| 4 |
Detlev Ganten, Klaus Ruckpaul: Encyclopedic reference of genomics and proteomics in molecular medicine
|
Read, Andrew
|
|
2007
|
121 |
6 |
p. 763-764
|
artikel
|
| 5 |
Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families
|
Bouzigon, Emmanuelle
|
|
2007
|
121 |
6 |
p. 711-719
|
artikel
|
| 6 |
Extreme individual marker FST values do not imply population-specific selection in humans: the NRG1 example
|
Gardner, Michelle
|
|
2007
|
121 |
6 |
p. 759-762
|
artikel
|
| 7 |
Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans
|
Reddy, M. V. Prasad Linga
|
|
2007
|
121 |
6 |
p. 721-727
|
artikel
|
| 8 |
Genetic association of IRF5 with SLE in Mexicans: higher frequency of the risk haplotype and its homozygozity than Europeans
|
Reddy, M. V. Prasad Linga
|
|
|
121 |
6 |
p. 721-727
|
artikel
|
| 9 |
Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation
|
Devlin, Bernie
|
|
2007
|
121 |
6 |
p. 675-684
|
artikel
|
| 10 |
Genome-wide linkage scan of prostate cancer Gleason score and confirmation of chromosome 19q
|
Schaid, Daniel J.
|
|
2007
|
121 |
6 |
p. 729-735
|
artikel
|
| 11 |
Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome
|
Reeuwijk, Jeroen van
|
|
2007
|
121 |
6 |
p. 685-690
|
artikel
|
| 12 |
Joe T. R. Clarke: A clinical guide to inherited metabolic diseases
|
Moat, Stuart
|
|
2007
|
121 |
6 |
p. 765
|
artikel
|
| 13 |
Linkage and association analysis of candidate genes for TB and TNFα cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes
|
Stein, Catherine M.
|
|
2007
|
121 |
6 |
p. 663-673
|
artikel
|
| 14 |
Mortality and cancer incidence in males with Y polysomy in Britain: a cohort study
|
Higgins, Craig D.
|
|
2007
|
121 |
6 |
p. 691-696
|
artikel
|
| 15 |
Parent–child pair design for detecting gene–environment interactions in complex diseases
|
Tan, Yuan-De
|
|
2007
|
121 |
6 |
p. 745-757
|
artikel
|
| 16 |
The P239S palladin variant does not account for a significant fraction of hereditary or early onset pancreas cancer
|
Zogopoulos, George
|
|
2007
|
121 |
6 |
p. 767
|
artikel
|
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