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Browsing by Author Loeys, B.

Full Text	Issue Date	Title	Author(s)
	2009	Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.	Bijlsma, E.K.; Gijsbers, A.C.; Schuurs-Hoeijmakers, J.H.M., 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
	2009	PORCN mutations in focal dermal hypoplasia: coping with lethality.	Bornholdt, D.; Oeffner, F.; Konig, A., et al