| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Barrett’s oesophagus: an ideal model to study cancer genetics
|
di Pietro, Massimiliano
|
|
2009
|
126 |
2 |
p. 233-246
|
artikel
|
| 2 |
Bayesian latent trait modeling of migraine symptom data
|
Chen, Carla Chia Ming
|
|
2009
|
126 |
2 |
p. 277-288
|
artikel
|
| 3 |
Detection of disease-associated deletions in case–control studies using SNP genotypes with application to rheumatoid arthritis
|
Wu, Chih-Chieh
|
|
2009
|
126 |
2 |
p. 303-315
|
artikel
|
| 4 |
Fiftieth anniversary of trisomy 21: returning to a discovery
|
Gautier, Marthe
|
|
2009
|
126 |
2 |
p. 317-324
|
artikel
|
| 5 |
Heike Allgayer, Helga Rehder and Simone Fulda: Hereditary tumours: from genes to clinical consequences
|
Davies, Mark
|
|
2009
|
126 |
2 |
p. 325
|
artikel
|
| 6 |
Novel human pathological mutations
|
Mohammed, Al Balwi
|
|
2009
|
126 |
2 |
p. 353
|
artikel
|
| 7 |
Novel human pathological mutations
|
|
|
2009
|
126 |
2 |
p. 329-352
|
artikel
|
| 8 |
Population programs for the detection of couples at risk for severe monogenic genetic diseases
|
Zlotogora, Joël
|
|
2009
|
126 |
2 |
p. 247-253
|
artikel
|
| 9 |
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
|
Hillmer, Axel M.
|
|
2009
|
126 |
2 |
p. 255-264
|
artikel
|
| 10 |
Strategies and issues in the detection of pathway enrichment in genome-wide association studies
|
Hong, Mun-Gwan
|
|
2009
|
126 |
2 |
p. 289-301
|
artikel
|
| 11 |
Terence J. Bazzett: An introduction to behavior genetics
|
Florio, Arianna Di
|
|
2009
|
126 |
2 |
p. 327
|
artikel
|
| 12 |
The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans
|
McDonough, Caitrin W.
|
|
2009
|
126 |
2 |
p. 265-275
|
artikel
|
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