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	1.	Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. Online. [electronic resource] by Ebhardt, M Schmidt, H Doerk, T Tietge, U Haas, R Manns, M P Schmidtke, J Stuhrmann, M Producer: 19990713 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Detection of 100% of the CFTR mutations in 63 CF families from Tyrol. [electronic resource] by Stuhrmann, M Dörk, T Frühwirth, M Golla, A Skawran, B Antonin, W Ebhardt, M Loos, A Ellemunter, H Schmidtke, J Producer: 19980121 In: Clinical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Delayed low density lipoprotein (LDL) catabolism despite a functional intact LDL-apolipoprotein B particle and LDL-receptor in a subject with clinical homozygous familial hypercholesterolemia. [electronic resource] by Schmidt, H H Stuhrmann, M Shamburek, R Schewe, C K Ebhardt, M Zech, L A Büttner, C Wendt, M Beisiegel, U Brewer, H B Manns, M P Producer: 19980702 In: The Journal of clinical endocrinology and metabolism vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis. [electronic resource] by Varret, M Rabés, J P Thiart, R Kotze, M J Baron, H Cenarro, A Descamps, O Ebhardt, M Hondelijn, J C Kostner, G M Miyake, Y Pocovi, M Schmidt, H Schuster, H Stuhrmann, M Yamamura, T Junien, C Béroud, C Boileau, C Producer: 19980218 In: Nucleic acids research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)