| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression
|
Cavalli, Marco
|
|
2016
|
135 |
5 |
p. 485-497
|
artikel
|
| 2 |
Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression
|
Cavalli, Marco
|
|
|
135 |
5 |
p. 485-497
|
artikel
|
| 3 |
Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies
|
Damiati, E.
|
|
2016
|
135 |
5 |
p. 499-511
|
artikel
|
| 4 |
Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies
|
Damiati, E.
|
|
|
135 |
5 |
p. 499-511
|
artikel
|
| 5 |
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
|
Ben Said, Mariem
|
|
2016
|
135 |
5 |
p. 513-524
|
artikel
|
| 6 |
Erratum to: Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast Asia
|
Brandão, Andreia
|
|
2016
|
135 |
5 |
p. 587
|
artikel
|
| 7 |
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue
|
Alazami, Anas M.
|
|
2016
|
135 |
5 |
p. 525-540
|
artikel
|
| 8 |
Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk
|
Tragante, Vinicius
|
|
2016
|
135 |
5 |
p. 453-467
|
artikel
|
| 9 |
Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk
|
Tragante, Vinicius
|
|
|
135 |
5 |
p. 453-467
|
artikel
|
| 10 |
MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients
|
Mouton, J. M.
|
|
2016
|
135 |
5 |
p. 477-483
|
artikel
|
| 11 |
No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients
|
Hutter, Sonja
|
|
2016
|
135 |
5 |
p. 469-475
|
artikel
|
| 12 |
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins
|
Szafranski, Przemyslaw
|
|
2016
|
135 |
5 |
p. 569-586
|
artikel
|
| 13 |
Polymorphisms in the MTHFR gene influence embryo viability and the incidence of aneuploidy
|
Enciso, María
|
|
2016
|
135 |
5 |
p. 555-568
|
artikel
|
| 14 |
Refining the Y chromosome phylogeny with southern African sequences
|
Barbieri, Chiara
|
|
2016
|
135 |
5 |
p. 541-553
|
artikel
|
| 15 |
Refining the Y chromosome phylogeny with southern African sequences
|
Barbieri, Chiara
|
|
|
135 |
5 |
p. 541-553
|
artikel
|
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