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Collins, F.A., Murphy, D.L., Reiss, A.L. Sims, K.B., Lewis, J.G., Freund, L., Karoum, F., Zhu, D., Maumenee, I.H. and Antonarakis, S.E. (1992) Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes. American Journal of Medical Genetics, 42, 127-134. doi:10.1002/ajmg.1320420126

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