A structural basis for reading fluency : White matter defects in a genetic brain malformation von CHANG, B. S, KATZIR, T, WALSH, C. A, LIU, T, CORRIVEAU, K, BARZILLAI, M, APSE, K. A, BODELL, A, HACKNEY, D, ALSOP, D, WONG, S

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Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia von CHANG, B. S, LY, J, GALABURDA, A. M, WALSH, C. A, APPIGNANI, B, BODELL, A, APSE, K. A, RAVENSCROFT, R. S, SHEEN, V. L, DOHERTY, M. J, HACKNEY, D. B, O'CONNOR, M

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A familial syndrome of unilateral polymicrogyria affecting the right hemisphere von Chang, B S, Apse, K A, Caraballo, R, Cross, J H, Mclellan, A, Jacobson, R D, Valente, K D, Barkovich, A J, Walsh, C A

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Living with Marfan syndrome: coping with stigma von Peters, KF, Apse, KA, Blackford, A, McHugh, B, Michalic, D, Biesecker, BB

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Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients von Apse, Kira A., Biesecker, Barbara B., Giardiello, Francis M., Fuller, Barbara P., Bernhardt, Barbara A.

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Living with Marfan syndrome: coping with stigma: Stigma in Marfan syndrome von Peters, KF, Apse, KA, Blackford, A, McHugh, B, Michalic, D, Biesecker, BB

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Dynactin helps target Polo-like kinase 1 to kinetochores via its left-handed beta-helical p27 subunit von Yeh, Ting-Yu, Kowalska, Anna K, Scipioni, Brett R, Cheong, Frances Ka Yan, Zheng, Meiying, Derewenda, Urszula, Derewenda, Zygmunt S, Schroer, Trina A

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