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Browsing by Author Martinet, D.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2009 | Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome. | Aa, N. van der; Rooms, L.; Weyer, G. van de, et al |
| 2011 | Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus | Jacquemont, S.; Reymond, A.; Zufferey, F., et al |
| 2011 | The phenotype of recurrent 10q22q23 deletions and duplications | Bon, B.W. van; Balciuniene, J.; Fruhman, G., et al |
| 2012 | Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial. | Hegi, M.E.; Janzer, R.C.; Lambiv, W.L., et al |
Showing results 1 to 4 of 4
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