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American Journal of Human Genetics|October 1, 1993
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndromeA McConkie-Rosell, A M Lachiewicz, G A Spiridigliozzi, et al.Clinical Genetics|July 1, 1992
Linkage analysis in properdin deficiency families: refined location in proximal XpC Wadelius, M Pigg, M Sundvall, et al.Pageof 3