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	51	What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases? Enthalten in Orphanet journal of rare diseases Bd. 16, 21.1.2021, Nr. 1, date:12.2021: 1-5
	52	Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia Enthalten in BMC cardiovascular disorders Bd. 14, 26.8.2014, Nr. 1, date:12.2014: 1-6