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Citation: K. Openo, Kimberly et al., Epimerase-Deficiency Galactosemia Is Not a Binary Condition, American journal of human genetics , 78(1), 2006, pp. 89-102

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Citation: E. Schnur, Rhonda et al., An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size using cloned DNA probes and flow cytometry, American journal of human genetics , 45-II(5), 1989, pp. 706-720