nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk
|
Carvajal-Carmona, Luis G. |
|
2014 |
134 |
2 |
p. 231-245 |
artikel |
2 |
Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome
|
Walz, Katherina |
|
2014 |
134 |
2 |
p. 181-190 |
artikel |
3 |
Effects of enamel matrix genes on dental caries are moderated by fluoride exposures
|
Shaffer, John R. |
|
2014 |
134 |
2 |
p. 159-167 |
artikel |
4 |
Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels
|
Hellwege, Jacklyn N. |
|
2014 |
134 |
2 |
p. 203-213 |
artikel |
5 |
Erratum to: Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels
|
Hellwege, Jacklyn N. |
|
2014 |
134 |
2 |
p. 215 |
artikel |
6 |
Genetic and environmental components of family history in type 2 diabetes
|
Cornelis, Marilyn C. |
|
2014 |
134 |
2 |
p. 259-267 |
artikel |
7 |
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium
|
Li, Qing |
|
2014 |
134 |
2 |
p. 131-146 |
artikel |
8 |
Loss-of-function mutation in the X-linked TBX22 promoter disrupts an ETS-1 binding site and leads to cleft palate
|
Fu, Xiazhou |
|
2014 |
134 |
2 |
p. 147-158 |
artikel |
9 |
Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland
|
Zhao, Li |
|
2014 |
134 |
2 |
p. 217-230 |
artikel |
10 |
Revisiting heritability accounting for shared environmental effects and maternal inheritance
|
Liu, Chunyu |
|
2014 |
134 |
2 |
p. 169-179 |
artikel |
11 |
The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy
|
Hosseini, S. Mohsen |
|
2014 |
134 |
2 |
p. 247-257 |
artikel |
12 |
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
|
Woodbury-Smith, Marc |
|
2014 |
134 |
2 |
p. 191-201 |
artikel |