Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits von MacDermot, Kay D., Bonora, Elena, Sykes, Nuala, Coupe, Anne-Marie, Lai, Cecilia S.L., Vernes, Sonja C., Vargha-Khadem, Faraneh, McKenzie, Fiona, Smith, Robert L., Monaco, Anthony P., Fisher, Simon E.

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Molecular evolution of FOXP2 , a gene involved in speech and language von Pääbo, Svante, Enard, Wolfgang, Przeworski, Molly, Fisher, Simon E, Lai, Cecilia S. L, Wiebe, Victor, Kitano, Takashi, Monaco, Anthony P

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A forkhead-domain gene is mutated in a severe speech and language disorder von Monaco, Anthony P, Lai, Cecilia S. L, Fisher, Simon E, Hurst, Jane A, Vargha-Khadem, Faraneh

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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder von Lai, Cecilia S. L., Gerrelli, Dianne, Monaco, Anthony P., Fisher, Simon E., Copp, Andrew J.

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Deciphering the genetic basis of speech and language disorders von FISHER, Simon E, LAI, Cecilia S. L, MONACO, Anthony P

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The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder von Lai, Cecilia S.L., Fisher, Simon E., Hurst, Jane A., Levy, Elaine R., Hodgson, Shirley, Fox, Margaret, Jeremiah, Stephen, Povey, Susan, Jamison, D. Curtis, Green, Eric D., Vargha-Khadem, Faraneh, Monaco, Anthony P.

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Definition of fibronectin-mediated uptake of gelatinized latex by liver slices and macrophages von Molnar, Janos, Galles, Mary, Beezhold, Donald, Lai, Ming Zong, Ku, Cecilia S-L, Van Alten, Pierson J.

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