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Browsing by Author Sharp, A.J.

Full Text	Issue Date	Title	Author(s)
	2007	Characterization of a recurrent 15q24 microdeletion syndrome.	Sharp, A.J.; Selzer, R.R.; Veltman, J.A., et al
	2008	Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.	Koolen, D.A.; Sharp, A.J.; Hurst, J.A., et al
	2012	Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction	Borel, C.; Cheung, F.; Stewart, H., 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	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