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Browsing by Author Sharp, A.J.
Showing results 3 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 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 | Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15. | Sharp, A.J.; Migliavacca, E.; Dupre, Y., et al |
| 2008 | Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. | Mefford, H.C.; Sharp, A.J.; Baker, C., et al |
Showing results 3 to 5 of 5
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