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Results: 2

Authors: He, M Rutledge, S.L. Palmer, C.A. Murdoch, G. Majumder, N. Nicholls, R.D. Pei, Z. Watkins, P.A. Vockley, J.
Citation: M. He, et al., A New Genetic Disorder in Mitochondrial Fatty Acid .-Oxidation: ACAD9 Deficiency, American journal of human genetics , 81(1), 2007, pp. 87-103

Authors: Chai, J-H. Locke, D.P. Greally, J.M. Knoll, J.H.M. Ohta, T. Dunai, J. Yavor, A. Eichler, E.E. Nicholls, R.D.
Citation: Chai, J-h et al., Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons, American journal of human genetics , 73(4), 2003, pp. 898-925
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