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Browsing by Author Bartholdi, D.

Full Text	Issue Date	Title	Author(s)
	2011	De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome	Hoischen, A.; Bon, B.W. van; Rodriguez-Santiago, B.; Gilissen, C.F.H.A.; Vissers, L.E.L.M., et al
	2004	Spinal phenotype of cerebrotendinous xanthomatosis--a pitfall in the diagnosis of multiple sclerosis.	Bartholdi, D.; Zumsteg, D.; Verrips, A.; Wevers, R.A.; Sistermans, E.A., et al