Characterization of cellular and neurological damage following unilateral hypoxia/ischemia von Olson, E.E., McKeon, R.J.

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High-speed AJL8/APC polymer modulator von Michalak, R.J., Ying-Hao Kuo, Nash, F.D., Szep, A., Caffey, J.R., Payson, P.M., Haas, F., McKeon, B.F., Cook, P.R., Brost, G.A., Jingdong Luo, Jen, A.K.-Y., Dalton, L.R., Steier, W.H.

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63 von McGrath, J A, Duijf, P H, Doetsch, V, Irvine, A D, de Waal, R, Vanmolkot, K R, Wessagowit, V, Kelly, A, Atherton, D J, Griffiths, W A, Orlow, S J, van Haeringen, A, Ausems, M G, Yang, A, McKeon, F, Bamshad, M A, Brunner, H G, Hamel, B C, van Bokhoven, H

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Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63 von Duijf, Pascal H. G., Vanmolkot, Kaate R. J., Propping, Peter, Friedl, Waltraut, Krieger, Elmar, McKeon, Frank, Dötsch, Volker, Brunner, Han G., van Bokhoven, Hans

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63 von MCGRATH, John A, DUIJF, Pascal H. G, ORLOW, Seth J, VAN HAERINGEN, Arie, AUSEMS, Margreet G. E. M, YANG, Annle, MCKEON, Frank, BAMSHAD, Michael A, BRUNNER, Han G, HAMEL, Ben C. J, VAN BOKHOVEN, Hans, DOETSCH, Volker, IRVINE, Alan D, DE WAAL, Rob, VANMOLKOT, Kaate R. J, WESSAGOWIT, Vesarat, KELLY, Alexander, ATHERTON, David J, GRIFFITHS, W. Andrew D

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Isolated Hypoglossal Nerve Palsy due to Compression by a Dissecting Vertebral Artery von McKeon, A., Murphy, S., McNamara, B., Ryder, D.Q., Galvin, R.J.

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