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Browsing by Author Anderlid, B.M.

Full Text	Issue Date	Title	Author(s)
	2008	Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.	Koolen, D.A.; Sistermans, E.A.; Nilessen, W., et al
	2012	Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.	Lindsay, M.E.; Schepers, D.; Bolar, N.A., et al
	2011	Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions.	Vergult, S.; Krgovic, D.; Loeys, B.L., et al
	2006	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.	Koolen, D.A.; Vissers, L.E.L.M.; Pfundt, R., et al