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Citation: S. Holve et al., Metachromatic leukodystrophy in the Navajo: Fallout of the American-Indianwars of the nineteenth century, AM J MED G, 101(3), 2001, pp. 203-208

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Citation: Bs. Andresen et al., Medium-chain Acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-Based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency, AM J HU GEN, 68(6), 2001, pp. 1408-1418

Authors: McCandless, SE Schwartz, S Morrison, S Garlapati, K Robin, NH

Citation: Se. Mccandless et al., Adult with an interstitial deletion of chromosome 10 [del(10)(q25.1q25.3)]: Overlap with Coffin-Lowry syndrome, AM J MED G, 95(2), 2000, pp. 93-98

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Citation: Ce. Ievers et al., Case studies: Psychological test findings for two children with X-linked adrenoleukodystrophy, J DEV BEH P, 20(1), 1999, pp. 31-35