| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients
|
Yu, Lei
|
|
2010
|
129 |
3 |
p. 335-344
|
artikel
|
| 2 |
A novel locus for disseminated superficial actinic porokeratosis maps to chromosome 16q24.1-24.3
|
Luan, Jing
|
|
2010
|
129 |
3 |
p. 329-334
|
artikel
|
| 3 |
Erratum to: Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
|
Mehmood, Tahir
|
|
2010
|
129 |
3 |
p. 271
|
artikel
|
| 4 |
Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes
|
Geremek, Maciej
|
|
2010
|
129 |
3 |
p. 283-293
|
artikel
|
| 5 |
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans
|
Lo, Ken Sin
|
|
2010
|
129 |
3 |
p. 307-317
|
artikel
|
| 6 |
Genetic variants in telomere-maintaining genes and skin cancer risk
|
Nan, Hongmei
|
|
2010
|
129 |
3 |
p. 247-253
|
artikel
|
| 7 |
Germline PKHD1 mutations are protective against colorectal cancer
|
Ward, Christopher J.
|
|
2011
|
129 |
3 |
p. 345-349
|
artikel
|
| 8 |
Insight into the biochemical characteristics of a novel glucokinase gene mutation
|
Shen, Yunfeng
|
|
2010
|
129 |
3 |
p. 231-238
|
artikel
|
| 9 |
Investigation of 15 of the top candidate genes for late-onset Alzheimer’s disease
|
Belbin, Olivia
|
|
2010
|
129 |
3 |
p. 273-282
|
artikel
|
| 10 |
Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis
|
Wiszniewski, Wojciech
|
|
2010
|
129 |
3 |
p. 319-327
|
artikel
|
| 11 |
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population
|
Li, Cong
|
|
2010
|
129 |
3 |
p. 239-246
|
artikel
|
| 12 |
Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome
|
Mehmood, Tahir
|
|
2010
|
129 |
3 |
p. 255-269
|
artikel
|
| 13 |
Transcriptomic analysis of cell-free fetal RNA suggests a specific molecular phenotype in trisomy 18
|
Koide, Keiko
|
|
2010
|
129 |
3 |
p. 295-305
|
artikel
|
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