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American Journal of Medical Genetics|September 20, 2000
Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: polymerase chain reaction-based assays to simplify genotypingP A Krakowiak, N A Nwokoro, C A Wassif, et al.
Journal of Lipid Research|September 1, 1985
Familial apolipoprotein A-I and C-III deficiency, variant IIE J Schaefer, J M Ordovas, S W Law, et al.
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