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Browsing by Author Aa, N. van der
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| 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 |
| 2009 | Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. | Bon, B.W.M. van; Mefford, H.C.; Menten, B., et al |
| 2010 | Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes. | Bruno, D.L.; Anderlid, B.M.; Lindstrand, A., et al |
Showing results 4 to 6 of 6
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