| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Additive effect of TAp63 deficiency on the adrenocortical dysplasia (acd) phenotype
|
O’Connor, Bridget C.
|
|
2011
|
22 |
11-12 |
p. 714-721
|
artikel
|
| 2 |
A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice
|
Wada, Kenta
|
|
2011
|
22 |
11-12 |
p. 693-702
|
artikel
|
| 3 |
A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse
|
Merath, Kate M.
|
|
2011
|
22 |
11-12 |
p. 661-673
|
artikel
|
| 4 |
Erratum to: Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
|
Reinholdt, Laura G.
|
|
2011
|
22 |
11-12 |
p. 692
|
artikel
|
| 5 |
Genetic dissection of testis weight in mice: quantitative trait locus analysis using F2 intercrosses between strains with extreme testis weight, and association study using Y-consomic strains
|
Suto, Jun-ichi
|
|
2011
|
22 |
11-12 |
p. 648-660
|
artikel
|
| 6 |
Hypomethylation of functional retrotransposon-derived genes in the human placenta
|
Macaulay, Erin C.
|
|
2011
|
22 |
11-12 |
p. 722-735
|
artikel
|
| 7 |
Identification of high-copper-responsive target pathways in Atp7b knockout mouse liver by GSEA on microarray data sets
|
He, Kan
|
|
2011
|
22 |
11-12 |
p. 703-713
|
artikel
|
| 8 |
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome
|
Duchon, Arnaud
|
|
2011
|
22 |
11-12 |
p. 674-684
|
artikel
|
| 9 |
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
|
Reinholdt, Laura G.
|
|
2011
|
22 |
11-12 |
p. 685-691
|
artikel
|
| 10 |
Targeted insertion of two Mthfr promoters in mice reveals temporal- and tissue-specific regulation
|
Pickell, Laura
|
|
2011
|
22 |
11-12 |
p. 635-647
|
artikel
|
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