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